26
26
Mar 30, 2018
03/18
by
CSPAN
tv
eye 26
favorite 0
quote 0
the fda has a role to play. we are considering what changes could make ingredient information more consumer friendly. in addition to readability, this includes considering whether alternative names for ingredients could be used so they are more understandable. we could consider whether the use of the name vitamin b6 or people b12 might help better understand what is in their food. public health implications will be included as we consider whether simpler names could be used. one such proposed change is in front of us right now. we have been conditioned -- use theed to alternative name for testing chloride to make it clear this is a salt. the petitioner argued some consumers associate chloride with chlorine bleach. the petitioner urged the fda consider how renaming might replacing sodium chloride with potassium chloride, which could provide health benefits. we need to finish our work on labeling. we recently issued a guidance document that provides flexibility on how labeling requirements can be implanted. it sho
the fda has a role to play. we are considering what changes could make ingredient information more consumer friendly. in addition to readability, this includes considering whether alternative names for ingredients could be used so they are more understandable. we could consider whether the use of the name vitamin b6 or people b12 might help better understand what is in their food. public health implications will be included as we consider whether simpler names could be used. one such proposed...
18
18
Mar 29, 2018
03/18
by
CSPAN2
tv
eye 18
favorite 0
quote 0
fda has a critical role to play in making this happen. improving the nutrition, the diet of americans would be another transformative effort toward reducing the burden of any chronic diseases ranging from diabetes to cancer to heart disease. the public health gains with such efforts would almost certainly toward -- the american college of cardiology estimated 22.4% of all male deaths and 20.7% of all female deaths in 2015 were attributable to four dietary factors. in the prevalence of obesity increasing 33.7% in 2007 and 2008 the 39.6% in 2015-2016 had an increase in children 16.8% to 18.5% over that same time. even as small advance in the nutrition of a single individual which might've only a limited effect in that persons life, the impact on a persons individual chronic risk for disease when aggregated over the population would have a massive impact across tens of millions of people. i feel strongly that fda can do more to -- reading healthier diets for themselves and their families. today chronic disease, diseases of the leading cause
fda has a critical role to play in making this happen. improving the nutrition, the diet of americans would be another transformative effort toward reducing the burden of any chronic diseases ranging from diabetes to cancer to heart disease. the public health gains with such efforts would almost certainly toward -- the american college of cardiology estimated 22.4% of all male deaths and 20.7% of all female deaths in 2015 were attributable to four dietary factors. in the prevalence of obesity...
18
18
Mar 29, 2018
03/18
by
CSPAN2
tv
eye 18
favorite 0
quote 0
fda has a critical role to play in making this happen. improving the nutrition, the diet of americans would be another transformative effort toward reducing the burden of many chronic diseases ranging from diabetes to cancer to heart disease. the public health gains would almost certainly door for any single medical innovation -- innovation we could consume, discovered. 22.4% 2.4% of all male deaths, and 20.7% of all female deaths since 2015 were attributable to poor dietary factors, and the prevalence of obesity in adults decreasing 33.7% in 2007-2008 to 39.6% in 2015-2016 had an increase in children 16.8% to 18.5% over that same time. even a small advance in the nutrition of a single individual which might've only a limited effect in that persons life, the impact on a persons individual chronic risk for disease when aggregate over the population would have a massive impact across tens of nice people. i feel strongly that fda could do more to assist the american public with trading healthier diets for themselves and their families. today
fda has a critical role to play in making this happen. improving the nutrition, the diet of americans would be another transformative effort toward reducing the burden of many chronic diseases ranging from diabetes to cancer to heart disease. the public health gains would almost certainly door for any single medical innovation -- innovation we could consume, discovered. 22.4% 2.4% of all male deaths, and 20.7% of all female deaths since 2015 were attributable to poor dietary factors, and the...
28
28
Mar 30, 2018
03/18
by
CSPAN
tv
eye 28
favorite 0
quote 0
when the fda has to change it two ways. a structure have where they will allow pharmaceutical companies to allow to make additional outcomes based on payment and the second thing is they need to have better collaboration with the knowledge base from the fda. da is about two years behind on issues. and don't have the staff they can't afford to compete with your company. what we have to do is have a collaboration rather than a relationship that is antagonistic. it needs to want -- it needs to be one of collaboration and how do we get the restaurants to the people. -- how do we get the best drugs to the people. i think we will solve those problems. we have spoken about value-based payments. if you describe about what you could wave your magic wand -- free at this time from stage four cancer -- prostate cancer. i don't need an immune treatment for my cancer. it hasn't been approved by the fda because it is in a study but the fact is that will be pretty expensive. if the fda would go back to what , what it will lower is the cost
when the fda has to change it two ways. a structure have where they will allow pharmaceutical companies to allow to make additional outcomes based on payment and the second thing is they need to have better collaboration with the knowledge base from the fda. da is about two years behind on issues. and don't have the staff they can't afford to compete with your company. what we have to do is have a collaboration rather than a relationship that is antagonistic. it needs to want -- it needs to be...
65
65
Mar 31, 2018
03/18
by
CSPAN
tv
eye 65
favorite 0
quote 0
so the fda has to change in two ways. they have to have a structure where they will allow pharmaceutical companies to make conditional outcomes based on payments. is, they needng to have better collaboration with a knowledge base that is of side the fda. i would tell you, the fda is behind in science on about two years on most issues. of what the leading edge is in all of this. it doesn't mean they're not smart, they just don't have the staff and cannot afford to compete with your company to put the staff there. so, what we have to do is have the collaboration, rather than a antagonistic relationship we had any to be one of collaboration and conciliation. how to get the most drugs to the best -- to the mostly black the cheapest cost. i think scott gottlieb will change this and if we allow drug companies to have innovations that are on a conditional basis of -- hey, he was outcome, no you get this many years to pay for it, that i think will solve those emblems. >> you have spoken about outcome based payments or value-based
so the fda has to change in two ways. they have to have a structure where they will allow pharmaceutical companies to make conditional outcomes based on payments. is, they needng to have better collaboration with a knowledge base that is of side the fda. i would tell you, the fda is behind in science on about two years on most issues. of what the leading edge is in all of this. it doesn't mean they're not smart, they just don't have the staff and cannot afford to compete with your company to...
48
48
Mar 28, 2018
03/18
by
CSPAN2
tv
eye 48
favorite 0
quote 0
the fda's judgment and i am so not speaking for fda. i think why dean is back there. but you know, the question is, do you need the ultimate answer on something like sodium reduction, which is admittedly a long-term problem to solve. you need a 10 year timeframe. you need to have all the science that has to understand not only what the ultimate end goal is get there to move to gauge you can make now. my perspective certainly is the science is more robust enough given what drives your guidelines to begin making gradual reductions when they can be made now towards an interim goal and do whatever science is needed. do whatever dialogue is needed to get a reasonable alignment on the science around the ultimate goal. but start moving down the pathway of what everybody agrees is a significant health issue. same people who claim what we are doing now is perfectly appropriate. that is not a consensus. another question here. these debates often happen around recommendation and somebody will point to a descending study. if you were fda you have to take the signs that his countr
the fda's judgment and i am so not speaking for fda. i think why dean is back there. but you know, the question is, do you need the ultimate answer on something like sodium reduction, which is admittedly a long-term problem to solve. you need a 10 year timeframe. you need to have all the science that has to understand not only what the ultimate end goal is get there to move to gauge you can make now. my perspective certainly is the science is more robust enough given what drives your guidelines...
52
52
Mar 9, 2018
03/18
by
CSPAN
tv
eye 52
favorite 0
quote 0
the fda approved the first flu vaccine manufactured using cell culture technology in 2012 and the fda approved the first flu vaccine manufactured using recombinant dna technology in 2013. in addition to new manufacturing technologies and methodologies, we've also seen new types of flu vaccine made available for the american people. historically, flu vaccines i understand have been offered to people to protect against three different stains of flu virus . and in 2012, the fda approved the first flu vaccine that offered protection against four different strains. in 2009, the fda approved the first high-dose flu vaccine for older adults, and some data show the high dose flu vaccine is more effective in older individuals than the normal dose. now that we have different ways to manufacture the flu vaccine, we need to have make sure we have enough data and information to make sure we're make the most effective seasonal flu vaccine possible. the fda recently announced that preliminary data shows cell-based flu vaccine might be more effective i understand in preventing the flu than the egg-ba
the fda approved the first flu vaccine manufactured using cell culture technology in 2012 and the fda approved the first flu vaccine manufactured using recombinant dna technology in 2013. in addition to new manufacturing technologies and methodologies, we've also seen new types of flu vaccine made available for the american people. historically, flu vaccines i understand have been offered to people to protect against three different stains of flu virus . and in 2012, the fda approved the first...
36
36
Mar 28, 2018
03/18
by
CSPAN2
tv
eye 36
favorite 0
quote 0
fda should wait for more research. on this particular issue and for obesity, the chronic disease obesity, diabetes and so forth, fda is not the greater science everybody knows. it's a science taker, particularly the dietary guideline process can translate that to make public health policy decisions. in the case of sugar labeling, the question was should we simply let consumers know the amount of added sugar in products in response to a dietary guideline recommendation that consumers reduce their calories from added sugar. i feel more free to say now than i did then, this is a no-brainer from fda standpoint. you know, we have the authoritative bodies that we need to reduce added sugar. the question was, do we have enough evidence to justify and certainly what we had with respect to the contribution of added sugar to obesity in at least some parts of the population, the nature density issues. we had plenty of science to require that declaration, even though we don't have all the science that fully understands the contrib
fda should wait for more research. on this particular issue and for obesity, the chronic disease obesity, diabetes and so forth, fda is not the greater science everybody knows. it's a science taker, particularly the dietary guideline process can translate that to make public health policy decisions. in the case of sugar labeling, the question was should we simply let consumers know the amount of added sugar in products in response to a dietary guideline recommendation that consumers reduce...
24
24
Mar 8, 2018
03/18
by
CSPAN2
tv
eye 24
favorite 0
quote 0
but he said i do not understand why the cdc and fda do not push a vaccine. it would seem to me that they might push for phase two and australia this year and possibly phase three in the united states. that could make it available starting in the fall of 2019. if the government is serious under serious about speeding up the approval process and i asked the question because it makes sense so why are we using the australian flu season to start testing these new ideas? that there are 40 new products out there could we shorten that time. if we did some of it here or there with the opposite seasons? >> i will comment briefly i have not familiar with the drug you think it is recombinant vaccine. >> i believe it is. but tested compared to the vaccine for senior adults of which i am rapidly approaching that category. [laughter] >> it isn't uncommon to see products tested in the southern hemisphere i'm not sure about that circumstance but that is a common phenomenon you will see them tested their. >> see you are not against it? mccue can pass on to anyone we will acti
but he said i do not understand why the cdc and fda do not push a vaccine. it would seem to me that they might push for phase two and australia this year and possibly phase three in the united states. that could make it available starting in the fall of 2019. if the government is serious under serious about speeding up the approval process and i asked the question because it makes sense so why are we using the australian flu season to start testing these new ideas? that there are 40 new...
159
159
Mar 16, 2018
03/18
by
KNTV
tv
eye 159
favorite 0
quote 0
the fda is now seeking to impose new limits on nicotine to make smoking less addictive. for more on this historic move, here's nbc's anne thompson. >> reporter: imagine lighting up with little or no risk of getting hooked. that's behind the fda's proposal to dramatically lower nicotine, the addictive ingredient in cigarettes. >> by regulating the nicotine and reducing it to levels that are minimally or nonaddictive, you can help break that cycle of addiction to tobacco. >> reporter: commissioner gottlieb points to a study in today's "new england journal of medicine" that says that cutting nicotine in cigarettes could save 8 million lives by the end of the century. >> this is the most dangerous legal product on the market. it's the only product that if used as intended is going to kill half of its users. >> reporter: cutting nicotine may also reduce the nearly $300 billion in healthcare and lost productivity cigarettes cost the economy every year and stop teen smokers from becoming adult smokers. >> this could completely change the future history of teen tobacco use. if a
the fda is now seeking to impose new limits on nicotine to make smoking less addictive. for more on this historic move, here's nbc's anne thompson. >> reporter: imagine lighting up with little or no risk of getting hooked. that's behind the fda's proposal to dramatically lower nicotine, the addictive ingredient in cigarettes. >> by regulating the nicotine and reducing it to levels that are minimally or nonaddictive, you can help break that cycle of addiction to tobacco. >>...
190
190
Mar 10, 2018
03/18
by
KNTV
tv
eye 190
favorite 0
quote 0
now it's selling the first fda-approved home test for breast cancer risk. the $200 kit can be bought without a prescription. it tests for three specific mutations including brca1 which causes 55% to 65% of women to develop cancer. ann mellinger took the test before fda approval and was shocked when it came back positive. she protectively had both her breasts and ovaries removed. >> it really is about taking control of your information and acting on it in the way that is right for you. >> reporter: but the test is limited, identifying only three mutations out of thousands. and genetic mutations only account for 5% to 10% of all breast cancer cases. >> everyone always thinks more information is better, but i think it's important that these test results can give misinformation as well. >> reporter: if someone tests positive -- >> sure. >> reporter: -- what would be your recommendation for them? >> my recommendation would be to proceed with caution. even the fda is recommending confirming these results. >> reporter: that's also recommended by the company. but m
now it's selling the first fda-approved home test for breast cancer risk. the $200 kit can be bought without a prescription. it tests for three specific mutations including brca1 which causes 55% to 65% of women to develop cancer. ann mellinger took the test before fda approval and was shocked when it came back positive. she protectively had both her breasts and ovaries removed. >> it really is about taking control of your information and acting on it in the way that is right for you....
41
41
Mar 12, 2018
03/18
by
CSPAN3
tv
eye 41
favorite 0
quote 0
it is critical to work with our counterparts at fda and hhs. i have the utmost respect for them and i look forward to working with them in the future. the only way we can tackle this problem is together. i came from a task force in new york city compromised of new york police. the only reason we were successful is we worked together. paranoia miss you any kind of scientific data, anything fda or hhs can bring to the table i will be more than happy to work with. >> the concern is to make sure you all make reasonable technical accommodations for research which is critical, and that fda should continue to have some role in the scheduling process. i appreciate your comments. what we hope is you all, the dea would, would help provide some technical comments to, in essence a bill, which is hr-2851 which i scribbled -- i don't like to use acronyms. i tried to describele down. stop imimportanttation and trafficking -- yes, you got it. >> if you can make toe suggestions and i think this bill will get a fair hearing and we would like to have entrepreneur
it is critical to work with our counterparts at fda and hhs. i have the utmost respect for them and i look forward to working with them in the future. the only way we can tackle this problem is together. i came from a task force in new york city compromised of new york police. the only reason we were successful is we worked together. paranoia miss you any kind of scientific data, anything fda or hhs can bring to the table i will be more than happy to work with. >> the concern is to make...
197
197
Mar 16, 2018
03/18
by
KSTS
tv
eye 197
favorite 0
quote 0
. >> por eso la fda (agencia de alimentos y medicamentos de estados unidos( que regula esta industria , dice que les baajran laran la nicotina . >> asi dicen que es el movimiento mas audaz hecho antes . >> carlos hernandez , habla de l la regualacion . >> uno debe calmar tambien la n aa ansiedad del cigarro . >> el consumo cuesta 300 mil millones de dolares al aÑo . >> a peasr de la fda (agencia de alimentos y medicamentos de estados unidos( en estados unidos todavia el 15% de la p poblacion fuma y cada aÑo pie e pierden la vida mas de 480 mil persona por ennfermedades . >> queirireren bajar el numero , 1,4% . >> hablamos con varias ciompaÑis de cigarros y cotnestaron . >> informacion en -- pantalla . >> aunque es solo el primer paso paso par a la a la fda (agencia alimentos y medicamentos de estados unidos( en nueva york , ,noticias telemundo . >> al regresar . >> indignacion por la brutal k gogo golpiza de un besiisbolista a n novia, cuenta que esta arrepen i arrepentido a telemundo . >> despues de un aÑo en el es espacio el astronauta no es i n identico a su hermano gemelo que
. >> por eso la fda (agencia de alimentos y medicamentos de estados unidos( que regula esta industria , dice que les baajran laran la nicotina . >> asi dicen que es el movimiento mas audaz hecho antes . >> carlos hernandez , habla de l la regualacion . >> uno debe calmar tambien la n aa ansiedad del cigarro . >> el consumo cuesta 300 mil millones de dolares al aÑo . >> a peasr de la fda (agencia de alimentos y medicamentos de estados unidos( en estados...
20
20
Mar 1, 2018
03/18
by
CSPAN2
tv
eye 20
favorite 0
quote 0
i want to focus on this issue of the fda and dea. for the scheduling of the approval for the scientific safety and advocacy. we need to try to keep people from taking the first dose and that is a whole set of problems. they have opioid type events. there is a certain factors within the step process to bring new drugs under the controlled substances act to. then the da that enforces the criminal and civil justice on a substances do they believe in order to strike a balance between addressing the risk posed by the illicit use and allowing the scientific research needed to develop new therapies the fda should continue to have some role. a task force in new york city, prized. to have reasonable tactical accommodations for research which is critical and then the fda should continue to have a role in the scheduling process. they would help to provide some technical comments. i tried to struggle it down but i can't read my writing so stop importation and trafficking. if you could provide us some feedback on how we could address this concern
i want to focus on this issue of the fda and dea. for the scheduling of the approval for the scientific safety and advocacy. we need to try to keep people from taking the first dose and that is a whole set of problems. they have opioid type events. there is a certain factors within the step process to bring new drugs under the controlled substances act to. then the da that enforces the criminal and civil justice on a substances do they believe in order to strike a balance between addressing the...
48
48
Mar 7, 2018
03/18
by
KNTV
tv
eye 48
favorite 0
quote 0
the fda give it the green light. scott budman joins us with the news and the warning. scott. >> reporter: cancer detection may be within spitting distance, literally. 23 and me says its test is step one in finding out if you might have cancer. cancer can strike any of us. now a silicon valley tech company wants to give you a direct way to find out if you have a gene mutation that could indicate a higher risk for certain types of cancers. 23 and me just got fda approval with your permission to analyze your genetic risk. >> we're looking at three mutations that are most common in people who cannot be jewish ancestry. these genes can increase your risk. >> reporter: it's the first test of its kind that you can take without a doctor's prescription. that doesn't mean the doctor shouldn't be involved. >> we have access to all these information. >> reporter: doctors say your physician is a necessary part of the process. >> you can fully counsel the patient, obtain the correct personal information and family history knowing how to interpret the information to see which test is
the fda give it the green light. scott budman joins us with the news and the warning. scott. >> reporter: cancer detection may be within spitting distance, literally. 23 and me says its test is step one in finding out if you might have cancer. cancer can strike any of us. now a silicon valley tech company wants to give you a direct way to find out if you have a gene mutation that could indicate a higher risk for certain types of cancers. 23 and me just got fda approval with your...
42
42
quote
eye 42
favorite 0
quote 1
fda approved for over 18 years.
fda approved for over 18 years.
62
62
Mar 16, 2018
03/18
by
FBC
tv
eye 62
favorite 0
quote 0
fda approved for over 14 years. ashley: there are report that is claim andrew mccabe, fbi director could be fired by the end of the day, former congressman jason chaffetz if he agrees? >> he would be able to keep the pension. i oversaw personnel management, he will keep that unless he was convicted of something severe like treason. he has done things that are wrong that are out there, we are looking forward to inspector general report that will come out soon, the offense of professional responsibility is he made a recommendation and now that's in direct to raise hands. stuart: gop is planning on rolling out phase two of the tax cut program in hopes to make -- part of it would be making cuts to individuals permanent as opposed to temporary. peter king, i'm sure you would like to see a fix to state and local salt nondeductibility, but to to tell you kevin brady said ain't going to happen, what say you? >> i'm sure kevin brady feels that way, we have a strong disagreement on this. once they open the door, i do all i ca
fda approved for over 14 years. ashley: there are report that is claim andrew mccabe, fbi director could be fired by the end of the day, former congressman jason chaffetz if he agrees? >> he would be able to keep the pension. i oversaw personnel management, he will keep that unless he was convicted of something severe like treason. he has done things that are wrong that are out there, we are looking forward to inspector general report that will come out soon, the offense of professional...
46
46
Mar 12, 2018
03/18
by
CNNW
quote
eye 46
favorite 0
quote 1
fda approved for over 14 years. >>> brits are pointing fingers for poisoning a former spy with a nerve agent.
fda approved for over 14 years. >>> brits are pointing fingers for poisoning a former spy with a nerve agent.
52
52
Mar 13, 2018
03/18
by
CNNW
quote
eye 52
favorite 0
quote 1
fda approved for over 14 years. >>> the breaking news this morning, we just learned that president trump has fired secretary of state rex tillerson. he will nominate the director of the cia mike pompeo to replace
fda approved for over 14 years. >>> the breaking news this morning, we just learned that president trump has fired secretary of state rex tillerson. he will nominate the director of the cia mike pompeo to replace
101
101
Mar 7, 2018
03/18
by
KNTV
tv
eye 101
favorite 0
quote 0
today the fda gave it the green light. the test was designed by the mountain view based company and targets genes that can increase occur risk of breast, ovarian or prostate cancer. both doctors and 23 and me say a physician is a necessary part of the process. >> you can obtain all the correct personal information and family history knowing how to interpret the information to see which test is appropriate for each patient. >> the fda says the test should not be used as a substitute for seeing is your doctor. >> this may be a glimpse into the future. driverless shuttles now being tested in the east bay. it's an office park called bishop ranch. shuttles have been given the okay to be tested on the streets there designed to take a passenger a short distance as a complement to public transportation. bishop ranch is home to at&t, chevron and ge, as well. >>> there's a new list in forbes tally of the richest people in the world. it includes a first, amazon founder jeff bezos is the world's first centi billionaire and worth more
today the fda gave it the green light. the test was designed by the mountain view based company and targets genes that can increase occur risk of breast, ovarian or prostate cancer. both doctors and 23 and me say a physician is a necessary part of the process. >> you can obtain all the correct personal information and family history knowing how to interpret the information to see which test is appropriate for each patient. >> the fda says the test should not be used as a substitute...
76
76
Mar 28, 2018
03/18
by
CNBC
tv
eye 76
favorite 0
quote 0
joining us is the morning's keynote speaker, fda commissioner dr. scott gottlieb. thank you for being here >> thanks for having me. >> you know, i don't want to front run your speech too much, but what do you plan to say today? >> we're going to talk about some of the things that we're working on at fda, some of our policy priorities, things we're doing ashtd tobacco regulation, trying to bring down the price of drugs and bring competition into the market. a lot of the policies that we've advanced and are going to be advancing to create incentives for new drug innovation and try to advance areas like gene therapy. we see a lot of opportunities to make the improvements in human health. >> we've talked to you about some of these initiatives. looking more broadly at your tenure in the time that you've been commissioner at the fda, some people thought you were going to be very pro pharma. what's happened is you have tackled inefficiencies that you have seen as a doctor and as someone who worked at the fda in the past how did you lay out your path and mission for what y
joining us is the morning's keynote speaker, fda commissioner dr. scott gottlieb. thank you for being here >> thanks for having me. >> you know, i don't want to front run your speech too much, but what do you plan to say today? >> we're going to talk about some of the things that we're working on at fda, some of our policy priorities, things we're doing ashtd tobacco regulation, trying to bring down the price of drugs and bring competition into the market. a lot of the...
102
102
Mar 7, 2018
03/18
by
KTVU
tv
eye 102
favorite 0
quote 1
but that's one of the things that we've demonstrated but the fda and submission and review process. consumers can understand information like this. >> the fda is letting folks know that this particular gene -- you test for two or three of them -- this particular mutation that causes the breast cancer is really a small percentage of the population. so what do you have to say towards that? >> these genes are commonly referred to as the founder mutations and they are most present in people with orb question gnaw see -- oshkenazi accident. most people don't know their history. people who have had cancer themselves should have the conversation with physicians. we're wanting to have an easy way for individuals who may not be eligible for those types of tests to have a screen that they can decide they want themselves and get that information. so that we can help detect people who otherwise go untested and therefore don't have the opportunity to have the information at a time when it could help them prevent and better manage the risks that comes from the genes. >> one of the services that 2
but that's one of the things that we've demonstrated but the fda and submission and review process. consumers can understand information like this. >> the fda is letting folks know that this particular gene -- you test for two or three of them -- this particular mutation that causes the breast cancer is really a small percentage of the population. so what do you have to say towards that? >> these genes are commonly referred to as the founder mutations and they are most present in...
33
33
Mar 1, 2018
03/18
by
CSPAN2
tv
eye 33
favorite 0
quote 0
in the face of this growing addiction crisis fda grants the product approval and with moderate or severe disorder as part of a contract -- complete treatment plan. and then to allow for once monthly dosing this will be distributed through a strict distribution system that is part of the risk evaluation program. the men mitigate serious harm to result in the intravenous administration by the patient. it must be certified and to verify directly to healthcare providers as they journey toward recovery is different access to all evidence-based treatment options is critical. this is one such option government policies impacting these treatments must adapt to ensure patients have access to new innovative medical technology. historically from the oral medication the controlled substance act directly to patients however as required by the fda approved schedule can only be through the provider and not directly to patients in recent years the distribution has evolved with the system practices purchasing from a distributor that allows the specialty pharmacies to ship a subscription to the provider a
in the face of this growing addiction crisis fda grants the product approval and with moderate or severe disorder as part of a contract -- complete treatment plan. and then to allow for once monthly dosing this will be distributed through a strict distribution system that is part of the risk evaluation program. the men mitigate serious harm to result in the intravenous administration by the patient. it must be certified and to verify directly to healthcare providers as they journey toward...
198
198
Mar 12, 2018
03/18
by
CSPAN3
tv
eye 198
favorite 0
quote 0
>> this project just got approved and it will be on the market -- >> by fda? that is different. >> that's right. so it is not right now in the market. it will be in the market starting in march. >> so i'm asking did cms give a coverage decision on it? >> not yet. >> because what we're finding in a lot of areas in health care right now as we get fda approved products, and then we get delayed payment decisions from cms which is preventing access to patients. so that is a big problem if that is the case, we need to -- i'd appreciate knowing about that because we try to have impact on that. and i was interested in your testimony about talking about continuing education for physicians. do you think -- is there anything the federal government can do to encourage maybe what i would call ground level training, which is not after people are already out of medical school and practicing, but i've been talking with the association of american medical colleges for example about implementing more training programs for assessing pain and properly treating pain in medical sch
>> this project just got approved and it will be on the market -- >> by fda? that is different. >> that's right. so it is not right now in the market. it will be in the market starting in march. >> so i'm asking did cms give a coverage decision on it? >> not yet. >> because what we're finding in a lot of areas in health care right now as we get fda approved products, and then we get delayed payment decisions from cms which is preventing access to patients. so...
107
107
Mar 20, 2018
03/18
by
FOXNEWSW
tv
eye 107
favorite 0
quote 0
companies and inquiring extensive fda testing before companies released new cigars. the fda admits these regulations will destroy companies and jobs, but they say it doesn't matter because there are lots of jobs in america. for real, you can read it. rocky patel is the most famous cigar maker in this country and he joins us tonight. thanks for coming on. >> thanks. >> tucker: did someone vote did voters say they wanted this? >> absolutely not. congressman never intended cigars to be regulated. they only intended smokeless and cigarettes to be regulated. the fda took it upon themselves to decide one glove fits all and start regulating the cigar industry. they didn't take the option to investigate and understand the nature of the industry. basically it's family owned businesses that have been making cigars over decades. the retailers are main street main street mom-and-pop industries that are selling premium cigars to adults. the average cigar smoker smokes one cigar per month. they're 24.45 years old. the cigars ar marketed in luxury magazines like "cigar aficionado"
companies and inquiring extensive fda testing before companies released new cigars. the fda admits these regulations will destroy companies and jobs, but they say it doesn't matter because there are lots of jobs in america. for real, you can read it. rocky patel is the most famous cigar maker in this country and he joins us tonight. thanks for coming on. >> thanks. >> tucker: did someone vote did voters say they wanted this? >> absolutely not. congressman never intended cigars...
34
34
Mar 1, 2018
03/18
by
CSPAN2
tv
eye 34
favorite 0
quote 0
d >> so this was in discussion with the fda. it's part of our risk evaluation and mitigation strategy program. because a lot of doctors, some of them didn't want to do the buy-in bill, and so there had to be another within a restricted distribution system. so ifl a doctor in utah wanted o prescribe -- [inaudible] they can contact when the specialty pharmacies that we are workingne with. it will get a named patient, prescription to be sent to the doctor for use only in the patient. >> one last thing. dr. mulder, thank you. i was a hospice consultant pharmacist for many years. quite often in congress we have the tendency to overreact and overdue pics you pointed out something is very important. there are people out there who truly need these drugs. we need to make sure they're going to be able to get them and have access to them. so thank you for pointing that out. >> amen. >> thank you, mr. chairman. i yield back. >> chair thanks a gentleman and does the gentleman from michigan we should be recognized? >> yes. >> five minutes. >>
d >> so this was in discussion with the fda. it's part of our risk evaluation and mitigation strategy program. because a lot of doctors, some of them didn't want to do the buy-in bill, and so there had to be another within a restricted distribution system. so ifl a doctor in utah wanted o prescribe -- [inaudible] they can contact when the specialty pharmacies that we are workingne with. it will get a named patient, prescription to be sent to the doctor for use only in the patient....
133
133
Mar 28, 2018
03/18
by
FOXNEWSW
tv
eye 133
favorite 0
quote 1
let's bring in the fda commissioner scott gottlieb. i wanted to ask you, sir, is the opioid crisis the worst thing you're dealing with? >> i think it's the biggest health crisis facing the agency. this began as a problem with prescription drug. we see people transitions to street drug. most of the new addiction still happening to people who are first exposed to opioids from a lawful prescription. we can try to cut down the new addiction by rationalizing prescribing. we have tools to do that. we've been focused on tphart of the mission. >> dana: president trump said recently and the attorney general talking about suing certain drug companies for problems possibly ones in the past. but is this a productive way to do it if you're also trying to work with though companies to find pharmaceutical alternatives to treat opioids or treat pain? >> well, litigations by the justice department, i think that we've all made mistakes in the past in terms of my agency as well, in terms of our view about the addictive potential of these drugs. i think w
let's bring in the fda commissioner scott gottlieb. i wanted to ask you, sir, is the opioid crisis the worst thing you're dealing with? >> i think it's the biggest health crisis facing the agency. this began as a problem with prescription drug. we see people transitions to street drug. most of the new addiction still happening to people who are first exposed to opioids from a lawful prescription. we can try to cut down the new addiction by rationalizing prescribing. we have tools to do...
32
32
Mar 30, 2018
03/18
by
CSPAN
tv
eye 32
favorite 0
quote 0
then we are working with the fda. you never want to jump ahead of the fda. they need to make their own decisions, but the fda is at least willing to discuss the possibility of an accelerated approval based on the safety and animal data. we are well into that. things are moving well. you don't read about in the newspapers because there is no zika rou -- around right now. with regard to ebola, we had one vaccine that was shown to be effective in a trial that is not really designed to definitively show effectiveness. right now, there's a trial going on in west africa comparing the adnovirus vector data.e, accumulating the short answer to your question is that we are on the road to a vaccine for both of those, even though you don't hear about it anymore because we are not in the middle of an outbreak. >> ok. i saw three questions going around. do you want to go ahead, from my left, down the road? shannon? did you want to start? [laughter] >> i am shannon. i was interested in hearing about access and affordability if wems of vaccines and see a vaccine for ebola o
then we are working with the fda. you never want to jump ahead of the fda. they need to make their own decisions, but the fda is at least willing to discuss the possibility of an accelerated approval based on the safety and animal data. we are well into that. things are moving well. you don't read about in the newspapers because there is no zika rou -- around right now. with regard to ebola, we had one vaccine that was shown to be effective in a trial that is not really designed to definitively...
90
90
Mar 13, 2018
03/18
by
KTVU
tv
eye 90
favorite 0
quote 0
is there anything that can be done because the fda does not necessarily regulate this? > >> there is no amount of safe asbestos in makeup. we are calling on claires to inform the customers that have purchased it that the product is unsafe and we are asking the fda to do further testing. >> is there something people can do? reach out to legislators? >> we encourage people to reach out to elected officials and ask them for better laws to protect consumers from asbestos in products. >> what would you say to their response? they say we stand by our products and we do not believe they have any asbestos in them. what do you say to that? >> the research that we did was by an accredited lab that followed procedures that we know to be the best procedures. at best their statement is misleading but our studies found these products contain asbestos. >> we encourage parents to be cautious with powdery makeup that can contain talc. >>> thank you. we want to show you where the snow is really coming down. look at that. these are pictures from immigrant gap along interstate 80. it is pa
is there anything that can be done because the fda does not necessarily regulate this? > >> there is no amount of safe asbestos in makeup. we are calling on claires to inform the customers that have purchased it that the product is unsafe and we are asking the fda to do further testing. >> is there something people can do? reach out to legislators? >> we encourage people to reach out to elected officials and ask them for better laws to protect consumers from asbestos in...
39
39
Mar 7, 2018
03/18
by
KPIX
tv
eye 39
favorite 0
quote 0
. >> reporter: now for the first time, the fda is allowing the mountain view company to test for brca mutations. >> they are applicable primarily for ashkenazi ancestry. >> reporter: it tests for three possible mutations only see in a small percentage of the population, something medical ethics professor david magnus worries will confuse at-home users. >> people will misunderstand and believe that because they test negatively, not positive for any of the three brca genes tested by the company that means they have a clean bill of health. >> reporter: he worries someone could still have another one of the thousands of brca genes that aren't covered by the take-home kit. >> for some people who might be getting this test, it may be harder to really interpret and understand those results. >> reporter: but company representatives say it's something they have already worked through with the fda. >> for some people who might be getting this test, it may be harder to really interpret it and understand the results. >> reporter: the kit will be available on the "23andme" website within the next
. >> reporter: now for the first time, the fda is allowing the mountain view company to test for brca mutations. >> they are applicable primarily for ashkenazi ancestry. >> reporter: it tests for three possible mutations only see in a small percentage of the population, something medical ethics professor david magnus worries will confuse at-home users. >> people will misunderstand and believe that because they test negatively, not positive for any of the three brca genes...
63
63
Mar 28, 2018
03/18
by
CNBC
tv
eye 63
favorite 0
quote 0
more "squawk" after this glomera gottlieb at the fda. more "squawk" after this when this bell rings... ...it starts a chain reaction... ...that's heard throughout the connected business world. at&t network security helps protect business, from the largest financial markets to the smallest transactions, by sensing cyber-attacks in near real time and automatically deploying countermeasures. keeping the world of business connected and protected. that's the power of and. at crowne plaza, we know business travel isn't just business. there's this. a bit of this. why not? your hotel should make it easy to do all the things you do. which is what we do. crowne plaza. we're all business, mostly. >>> get this, there are two dow stocks in the green since the market topped out back in january. find out what they are and if they're worth your money on tradingnation.cnbc.com more "squawk on the street" ahead. today, a focus on innovation in the southern tier is helping build the new new york. starting with advanced manufacturing that brings big ideas t
more "squawk" after this glomera gottlieb at the fda. more "squawk" after this when this bell rings... ...it starts a chain reaction... ...that's heard throughout the connected business world. at&t network security helps protect business, from the largest financial markets to the smallest transactions, by sensing cyber-attacks in near real time and automatically deploying countermeasures. keeping the world of business connected and protected. that's the power of and. at...
92
92
Mar 29, 2018
03/18
by
CSPAN2
tv
eye 92
favorite 0
quote 0
the fda is the regulatory institute. it's really quite synergistic. we have worked work very closely with the cdc because whenever there's an outbreak that's the reason during ebola and zika you saw tom friedman and i talking about it. >> when you show those maps of the outbreaks in the models that the cdc created? >> yeah. >> thank you. >> you talk about moving away from the tech base but how long do you think, how long will we do this particularly what do you think it's save-- gets you there? >> that's a good question and it's a combination of the science proving that the other methods work. if you look this year we have one candidate using molecular biological techniques and that is the flu block vaccine. only about 3% of all the vaccine doses that were administered this year in this country were of that type. the overwhelming majority were egg-based and a lesser amount of cell-based. the first step in answering your question is have a few platforms that prove that they are as good or better than the egg-based and i think it won't do that much of a
the fda is the regulatory institute. it's really quite synergistic. we have worked work very closely with the cdc because whenever there's an outbreak that's the reason during ebola and zika you saw tom friedman and i talking about it. >> when you show those maps of the outbreaks in the models that the cdc created? >> yeah. >> thank you. >> you talk about moving away from the tech base but how long do you think, how long will we do this particularly what do you think...
57
57
Mar 21, 2018
03/18
by
KNTV
tv
eye 57
favorite 0
quote 0
the hotel room. >> oh, my goodness. >> because it was so important for her to be from front of that fda and get the approval for a ground breaking drug that would help save lives. that's exactly what happened. >> she's an inspiration to a lot of people. >> thank you, garvin. >>> get a check -- >> talk about the bay area connection to the royal wedding. this is big, janelle. prince harry and his bride, meghan markle, chose this woman to make her wedding cake. claire ptak, got her start in berkeley. she's the owner of violet bakery in london, the couple picked the lemon elderflower cake for the big day. prince harry confirmed the choice this morning. i have never had that kind of cake. >> me either. >> i'm interested. >> royal wedding, just one flavor? they should have a variety. >> it will probably be a j gigantic cake. >> perfect for a spring wedding. >> jeff, let's take a look at the forecast, spring officially right today? >> yes, it arrived this morning. >> 5:15. >> around 9:00 this morning. it's here, spring's here. we've got the rain coming in, and we do have some active weather ov
the hotel room. >> oh, my goodness. >> because it was so important for her to be from front of that fda and get the approval for a ground breaking drug that would help save lives. that's exactly what happened. >> she's an inspiration to a lot of people. >> thank you, garvin. >>> get a check -- >> talk about the bay area connection to the royal wedding. this is big, janelle. prince harry and his bride, meghan markle, chose this woman to make her wedding...
161
161
Mar 3, 2018
03/18
by
WPVI
tv
eye 161
favorite 0
quote 0
lyrica is fda approved to treat this pain, from moderate to even severe diabetic nerve pain. lyrica may cause serious allergic reactions, suicidal thoughts or actions.yif you have these, new or worse depression, unusual changes in mood or behavior, swelling, trouble breathing, rash, hives, blisters, muscle pain with fever, tired feeling or blurry vision. common side effects: dizziness, sleepiness, weight gain, swelling of hands, legs, and feet. don't drink alcohol while taking lyrica. don't drive or use machinery until you know how lyrica affects you. those who have had a drug or alcohol problem may be more likely to misuse lyrica. now i have less diabetic nerve pain. and i love smoothing the road ahead for others. as hey, what are you guys doing here? we're voya. we stay with you to and through retirement. so you'll still be here to help me make smart choices? well, with your finances that is. we had nothing to do with that tie. voya. helping you to and through retirement. you or joints. something for your heart... but do you take something for your brain. with an ingredient
lyrica is fda approved to treat this pain, from moderate to even severe diabetic nerve pain. lyrica may cause serious allergic reactions, suicidal thoughts or actions.yif you have these, new or worse depression, unusual changes in mood or behavior, swelling, trouble breathing, rash, hives, blisters, muscle pain with fever, tired feeling or blurry vision. common side effects: dizziness, sleepiness, weight gain, swelling of hands, legs, and feet. don't drink alcohol while taking lyrica. don't...
103
103
Mar 21, 2018
03/18
by
KTVU
tv
eye 103
favorite 0
quote 0
.>>> the fda taking aim at cigarettes including menthol. the government moves to curb smoking and raping among americas.>>> bring out there so, will have the forecast for your commute for your wednesday.>>> ended three minutes delta airline sent a puppy on a long and unnecessary trip as united makes the decision about its pets travel program. at&t has a network with thousands of best-in-class security experts. which means... more of the eye balls you want watching the network... & less of the ones you don't. more experts preventing security issues... & less security threats impacting our customers. more of a highly secure network with more security products available for further protection... & less per month. switch to at&t internet for business. more & less - that's the power of &. >>> a fire at a vacant warehouse this afternoon, employees first called in the fire this afternoon at west st. john and n. montgomery st. there was heavy smoke and flames when they arrived and took up a defensive stance. officials say the building was empty and
.>>> the fda taking aim at cigarettes including menthol. the government moves to curb smoking and raping among americas.>>> bring out there so, will have the forecast for your commute for your wednesday.>>> ended three minutes delta airline sent a puppy on a long and unnecessary trip as united makes the decision about its pets travel program. at&t has a network with thousands of best-in-class security experts. which means... more of the eye balls you want watching...
102
102
Mar 16, 2018
03/18
by
KNTV
tv
eye 102
favorite 0
quote 0
now the fda says it wants to cut down cravings by cutting out 30% of the nicotine. the fda has not made any final decisions about when this plan will roll out. >>> today is a big day in law enforcement as laura garcia, my co-anchor of "today in the bay" and myself got a chance to emcee the 55th annual law enforcement appreciation. this was a big event. so many people, you can see laura and me right there, a fun time. we honored so many of those officers, about 17 groups there, some single, two, or three. they did everything from their flight rescues in the north bay wildfires to even rescuing people from burning cars down an embankment. these officers do so much in our community. we want to thank them for all that they do. not only those honored today but those throughout the bay area. thank you, we can't say that enough, for all that you do to keep us safe. >> for sure, we appreciate your service and your dedication to the community. >>> you've been very busy. "today in the bay," you emceed that appreciation event and now you're here with us. >> and i'm happy. >> i
now the fda says it wants to cut down cravings by cutting out 30% of the nicotine. the fda has not made any final decisions about when this plan will roll out. >>> today is a big day in law enforcement as laura garcia, my co-anchor of "today in the bay" and myself got a chance to emcee the 55th annual law enforcement appreciation. this was a big event. so many people, you can see laura and me right there, a fun time. we honored so many of those officers, about 17 groups...
59
59
Mar 21, 2018
03/18
by
KGO
tv
eye 59
favorite 0
quote 0
. >>> and the new way the fda is considering regulating cigarettes. cigarettes. i go with anoro. ♪go your own way copd tries to say, "go this way." i say, "i'll go my own way" with anoro. ♪go your own way once-daily anoro contains two medicines called bronchodilators, that work together to significantly improve lung function all day and all night. anoro is not for asthma . it contains a type of medicine that increases risk of death in people with asthma. the risk is unknown in copd. anoro won't replace rescue inhalers for sudden symptoms and should not be used more than once a day. tell your doctor if you have a heart condition, high blood pressure, glaucoma, prostate, bladder, or urinary problems. these may worsen with anoro. call your doctor if you have worsened breathing, chest pain, mouth or tongue swelling, problems urinating, vision changes, or eye pain while taking anoro. ask your doctor about anoro. ♪go your own way get your first prescription free at anoro.com. inside all of us is a compass. and it always points true north. toward mountains of sand. toward new site
. >>> and the new way the fda is considering regulating cigarettes. cigarettes. i go with anoro. ♪go your own way copd tries to say, "go this way." i say, "i'll go my own way" with anoro. ♪go your own way once-daily anoro contains two medicines called bronchodilators, that work together to significantly improve lung function all day and all night. anoro is not for asthma . it contains a type of medicine that increases risk of death in people with asthma. the...
46
46
Mar 7, 2018
03/18
by
KPIX
tv
eye 46
favorite 0
quote 0
>> reporter: but the representatives say it is something they have already worked through with the fda. >> for some people who might be getting this test, it may be harder to interpret it and understand those results. >> reporter: but the testing kit will be available on the 23 and me website for the next couple of weeks. the cost, $199. in mountainview, katie nielsen, kpix 5. >> the brca test is a part of the whole genetic test that helps your heritage. you have to opt in, it is not automatic. >> how do you clean the bay area's tallest building? kpix 5 wilson walker, went to the very top of the sales floor tower in san francisco. and shows us the innovative tool that gives the exterior a custom cleanup job. >> well, when you get this tall in a building like this, you are over a thousand feet off the ground. even the simplest thing becomes very complicated. >> reporter: the simple thing we're talking about is cleaning ever 1 floors worth of windows on the -- cleaning 61 floors of the windows. >> and bmu is the acronym that they use for building maintenance unit. >> reporter: not just o
>> reporter: but the representatives say it is something they have already worked through with the fda. >> for some people who might be getting this test, it may be harder to interpret it and understand those results. >> reporter: but the testing kit will be available on the 23 and me website for the next couple of weeks. the cost, $199. in mountainview, katie nielsen, kpix 5. >> the brca test is a part of the whole genetic test that helps your heritage. you have to opt...
111
111
Mar 16, 2018
03/18
by
KGO
tv
eye 111
favorite 0
quote 0
. >>> the fda makes a move to change how cigarettes are made. a new push to make smoking less addictive. >>> plus, the wild upsets as march madness tips off. >>> walmart's bold plan to build an army of robotic bees. >>> how would you like to run into this guy at the beach? >>> a good friday morning, everyone, and we begin with several new developments. >>> moments ago authorities confirmed at least six people have been killed after that bridge came crashing down onto the highway below. there are reports that the cables had loosened and were being tightened at the time. >> we're now hearing from first responders who desperately tried to save workers trapped in the rubble. others pulled people out of crushed cars even using a wooden stick to rescue someone at some point. abc's maggie rulli is at the scene. maggie. >> reporter: diane and kendis, right behind me you can see the destruction. this massive bridge now just crumbled concrete scattered across the eight-lane highway. overnight rescue crews were desperately searching for survivors, but now
. >>> the fda makes a move to change how cigarettes are made. a new push to make smoking less addictive. >>> plus, the wild upsets as march madness tips off. >>> walmart's bold plan to build an army of robotic bees. >>> how would you like to run into this guy at the beach? >>> a good friday morning, everyone, and we begin with several new developments. >>> moments ago authorities confirmed at least six people have been killed after that...
51
51
Mar 7, 2018
03/18
by
KNTV
tv
eye 51
favorite 0
quote 0
today a green light from the fda. our business and tech reporter scott budman joins us from 23 and me headquarters right there in mountain view with this pivotal decision. scott? >> reporter: good morning, raj. this could mean a new way to detect genetically whether we are at risk for getting cancer. 23 and me calls it one step in the process. doctors say they want to be involved as well. 23 and me, which just last year got approval to include some health risk information, alongside genetic profiles, has a direct way to find out if you have a gene mutation that can show a risk for certain types of cancers. >> specifically we can tell people about risks for breast, ovarian and prostate cancer. >> reporter: now with fda approval, it's the first test of its kind that you as a consumer can take without a doctor's prescription. >> i think it's great that we have access to all this information. >> reporter: but doctors say they should be involved in the process as well. >> where you can fully counsel the patient, obtain all
today a green light from the fda. our business and tech reporter scott budman joins us from 23 and me headquarters right there in mountain view with this pivotal decision. scott? >> reporter: good morning, raj. this could mean a new way to detect genetically whether we are at risk for getting cancer. 23 and me calls it one step in the process. doctors say they want to be involved as well. 23 and me, which just last year got approval to include some health risk information, alongside...
76
76
Mar 7, 2018
03/18
by
KTVU
tv
eye 76
favorite 0
quote 0
today, the fda gave 23 and me the okay to sell the test directly to consumers. the test detects three mutations and a common type of breast cancer gene. earlier, we spoke to kathy hibbs, chief legal and regulatory officer from 23 and me. >> you spit into a tube, send it to us and it's processed through a laboratory, and then we return the information to you through your account. >> she says the test results take 4 to 6 weeks. the tests cost nearly $200. the fda says there are many mutations that the test doesn't detect and it should not be a substitute for going to the doctor. >>> the bay area on track with driverless vehicles. >> this is a big step. >> the east bay location where the vehicles are now street legal. >>> and, we will be getting the umbrellas out again pretty soon. not necessarily tomorrow, but toward the end of the day. we will look at the latest computer models and time it out for you. at&t has a network with thousands of best-in-class security experts. which means... more of the eye balls you want watching the network... & less of the ones you d
today, the fda gave 23 and me the okay to sell the test directly to consumers. the test detects three mutations and a common type of breast cancer gene. earlier, we spoke to kathy hibbs, chief legal and regulatory officer from 23 and me. >> you spit into a tube, send it to us and it's processed through a laboratory, and then we return the information to you through your account. >> she says the test results take 4 to 6 weeks. the tests cost nearly $200. the fda says there are many...
175
175
Mar 2, 2018
03/18
by
WPVI
tv
eye 175
favorite 0
quote 0
and itly tells the user normal o the fda approved the cardid for sale next fall. >>> and students are practicing their rhyming and readings today in honor of dr. school readi of green egg and a dr. seussye's song can't t futures, ing part in the second annual career day and more than 40 pionals spent d co wide variety ofel education and the public service sectors.heey canurchool and taction today at 4:00. >> happy friday.story you will love in our newscast today at 4:00 when a their favorite teach a tragedy stepis wife a not even 24 hours later the teaced a plan to pay itforward and " therein eens big surprise was. this one will melt your hearttodand lets talk about digital detox. why so many people are phone a device nicknam . we'l in big t at >> the dumyes. >> okay. thank you. breakaccuweather forecast with ssa magee is right around the corner. >>> meteorologist, melissa magee is back now way check of a dreary forecast out there. some folks are dealing with onsng >> i thinknd evening commute is a concern wet w .f trees winds as 35 miles per hour in kent county. and they will get hig
and itly tells the user normal o the fda approved the cardid for sale next fall. >>> and students are practicing their rhyming and readings today in honor of dr. school readi of green egg and a dr. seussye's song can't t futures, ing part in the second annual career day and more than 40 pionals spent d co wide variety ofel education and the public service sectors.heey canurchool and taction today at 4:00. >> happy friday.story you will love in our newscast today at 4:00 when a...