food and drug administration. the u.s. government expects a decision in the midst of december the 6th and now but coming up next, rock climbing becomes an olympic sport in our show. sports live coming up next and up next. and remember, you can keep up to date on our web site. e.w. dot com. i am told me the logical fix watching is for me, greta is for you 3 frito is truth.

food and drug administration for emergency approval of a covert 19 vaccine. it comes after the companies posted promising results from advanced trial. it showed a 94 percent success rate in adults over $65.00 and the park 89 months. after the start of this project, we have a readiness to bite you for sure and get approved. 4 boxes will be safe because it definitely is something that will redefine your interest. it will start the clock on a process that could save the vaccine approved for use in the u.s. by mid december. once approved, distribution will become the focus. and there's a mixed response from americans as to whether or not they will get the shot. of course. yeah. only sort of possible. and not really to say that i'm going to get a flu shot myself just because i'm out means system that been really good. how a yes or no, i'm not personally feel like so i guess everybody's own choice, you know, because not everybody agrees with vaccines, but experts don't want people getting too excited. stressing that the manufacture and distribution of the vaccine i

. >> peter, peter, it was the food and drug administration. the food and drug administration. >> bob, do not interrupt me on this, let me finish this point. the latest study that has come out on this has shown unequivocally that hydroxy clerk when works in early -- hydroxychloroquine works in early treatment to save lives. here's what i can tell you. we have 63 million tablets of hydroxychloroquine sitting in that strategic national stockpile. that is enough for 4 million americans treated in early treatment. that is enough to cut the death rate of people infected by 20% -- 20,000-30,000 american lives. and to be one of the biggest tragedies of this whole politicization of the pandemic has been the suppression of the use of a $12 drug that could have saved countless lives. so if you're asking me about the hydroxychloroquine, it is setting there not saving lives. because the mainstream media created a hysteria about it. when the science now, bob, the science is unequivocal, it works in early treatment to save lives. acknowledgeuld you that, and

a pproves food and drug administration approves those vaccines when it meets on the 10th of decemberm 95% effective in our priority report is to saying that it will be given to health workers front—line workers as they are called here and two members of the elderly. the elderly population indeed, very exciting development indeed. it is still worrying that 10% of people saying they are not going to take up the vaccine when it is offered to them and the doctor has said that when it was turned around so quickly, record timing. instead of ten years, less than a year. the effectiveness should not worry people, the effectiveness is there but the safety should not worry people. are americans like me to take this on board? i think like me to take this on board? ithinka like me to take this on board? i think a lot of them will. they're still those who are very doubtful about vaccines in general and a lot of conspiracy theories continue to rage in that regard. but many will take to heart the word of the health worker who has personally said that he will be taking the vaccine when it becomes av

say, i love them, it down to the point about nanami of being this has it and is about as a drug administration comes one, then those who dreamed up and executed the russia gate hoax ever be held accountable when the media ever be held accountable. for the role they play and should be now assume the deep state is truly above the law. because schumann's wiggin for, you know, millions of years to build up an emotional one. when the communication happens within 10 milliseconds in stipends zoom and all that after that because it takes about $260.00 milliseconds. just flip to talk. now when you get to the same room, you know, this emotional bond between us is very different and slyness. will bring this back to an disqualify stowell when you know 5th, you just all come to know they say all those things to me. so she was training to be a dog handler and all her classmates and teachers know she has a wolf. so during classes, they talk about the animal from a professional perspective. and i'm like, you know what, it's not that i no idea what you mean with losing and when it's just a little bump so good.

food and drug administration. u.s. government expects a decision and need to send out a forget you can always get the w. news on the go. you just download out at, from google play or from the out store. and that will give you access to all the lead. this news and information from around the world as well as push notifications for any breaking news and if your part of a news story, you can also use the app to send us photos and videos of what's happening in the, make of the filling up next here on the w., it's have reporters series on like question. we introduce you to a 14 year old who is fighting the effects of climate change in the caribbean. now you can also follow us on twitter and instagram on the social channels. the handle is at news for now though, from in the team here involved in the math anyhow. thanks which why are people forced to hide in trucks? there are many reasons. there are many answers and there are many stories make up your own made for minds. that turquoise seatback, kansas. with the promise of a

ago, democratic governor in new york and california both began second-guessing the food and drug administration and doubting its ability to assess the safety of a vaccine. suggesting blue states may said their own review boards and withhold lifesaving vaccines from their own people. for who knows how long until this extra obstacle had been hurdled. this is where they are. if over horgan is president until new york and california reinvent their own fda. to be clear, nearly 4 billion prescriptions every single year. 4 billion prescriptions. testing the expertise and professionalism of the fda. that is the trusted authority. nobody is crying out for liberal governors to have approval let alone potentially delay the end of covid-19 to do so. with the vaccine proves to be the one citizens in new york and california should not have it withheld because the governors care more about opposing president trump than about this. it reminds me when the senator from california declared in september during our vice presidential campaign that you might hesitate to trust a vaccine. the whole country understands

says its covid vaccine is 90% effective now the company has to submit its data to the food and drug administration. reporter basal john has more on why health experts are optimistic about this particular vaccine. >>i think it's a great. a great first step upstate medical university infectious disease chief doctor steven thomas. >>says he's encouraged by news that pfizer's trials show their vaccine is 90% effective may soon be ready for approval by the food and drug administration but think that it exceeded the expectations of lots of. >>vaccine developers and immunologist and clinicians after approval pfizer will shift toward manufacturing and distributing the vaccine there could be a significant role out of vaccine by the first or 2nd quarter of calendar year 21, however, one major distribution challenge. the vaccine needs to be stored at 94 degrees below 0 and not every hospital has the required equipment you have to understand verified you got the good side to take care of the vaccine to make sure that is going to still be efficacious when you're administering it to be out to the general public

ventaja la tiene pfizer que estarÁ disponible a partir del 12 de diciembre si la fda (food and drug administratione los sistemas de salud mÁs grandes e importantes del paÍs estÁn listos para recibir la vacuna de pfizer cuando sea autorizada y se han equipado con congeladores Última frÍo para esta vacuna que requiere una temperatura extremadamente baja. >> la seguridad de la vacuna divide opiniones >> no me la pondrÍa hasta que hubiera un poquito mÁs de estudios >> karina que trabaja de marzo en un piso de enfermos de covid-19, tiene confianza en las autoridades sanitarias >> la vacuna yo creo que es segura, no creo que van a poner algo que no es seguro. >> la principal discusiÓn sobre la vacuna se deriva del tiempo que se ha realizado porque generalmente toma algunos aÑos desarrollar una y esta ha seguido un proceso expreso, en diciembre la fda (food and drug administration) dirÁ si a prueba la vacuna de pfizer, pero tiene que ser efectiva y muy segura. >> increÍble lo rÁpido que esta llegando estas tres vacunas ¿no >> asÍ es. >> rogelio mora-tagle muchas gracias a pesar del riesgo de contagio y a

food and drug administration could grant permission before testing is complete. and if it does, the 1st doses could be administered as early as next month. now across the world, the severe health an economic impacts of the pandemic mean a vaccine can't come soon enough. a small pub with a big history 60 years of just the one of the albatross pub in california, once hosted intellectuals of the free speech movement in the sixty's today is shutting down for good jude to the coronavirus pandemic. where people came. everybody came to hang out and talk and it was a, it was a public space. it was, a user community space. it's a familiar story, not just in the u.s., but all across the world. the lives of many opened up ended by the pandemic. but on friday, some good news. german drug developer by own tech and its american partner, pfizer announced that they will be asking the u.s. food and drug administration for emergency approval of a covert. 19 vaccine comes after the companies posted promising results from advanced trial. it showed a 94 percent success rate in adults

food and drug administration. the u.s. government expects a decision. you need to see, but that's it for now, i can get up next here on day w, a weekly wrap of all world news. indeed, weekend reports for now, but from the team here in berlin, thanks. which we know this is very time for the coronavirus is changing the world, changing our lives. so take care of yourself. keep your distance, wash your hands. if you can stay at how we are here for you. we are working hard listening to keep you informed. don't overwhelm, we're all in this together. on together. make it. stay safe, everybody. stay safe. stay safe, priest, stay safe. let me put it this week on the world story. it's another strict lockdown in france. fighting indifference to corona in turkey. but our journey begins in the usa, the city of el paso, texas is one of the country's carona hot spots stretching hospitals and funeral homes there to their limits. and basso is on the border with mexico. but no one is talking about the wall anymore. the pandemic is raging here. numbers are sorie. right no

if approved by the food and drug administration, it could be distributed by early or late december. the company say trials indicate their vaccine is 95 percent effective. and there's hope from other drugs firms. the u.s. drugs maker is also expected to apply for emergency approval. this week the company said its vaccine is 95 percent effective in trials astra zeneca oxford university plan to release results of very late stage trials before christmas. and russia says its 5 vaccine is 92 percent effective. the w.h.o. is in talks with moscow over a potential application for emergency approval. that was the day as ever the conversation continues online at the w. . i'm a good luck . charm and cattle to limit the power of the book. to almost plug in hybrid cars. the choice of good looks sexy. read some good looks here and more beer. what else is there today? i want to find out what munich's got to offer for turner. it's fun to come here for a change. how about chimps and art history and culture music's got something well the 60 minutes p.w. told nico piece in germany to learn german, publi

food and drug administration for emergency approval of a coded 19 vaccine. comes after the companies posted promising results from advanced trial. it showed a 94 percent success rate in adults over $65.00 and the park 89 months. after the start of this project, we have a readiness to buy new fire. sure and get approved for boxes of this. as you can see, definitely it is something of a will redefine it will start the clock on a process that could save the vaccine approved for use in the u.s. by mid december. once approved, distribution will become the focus. and there's a mixed response from americans as to whether or not they will get the shot. of course. yeah. only sort of possible. and not really just i don't even take it beautifully, shot myself just because i'm out means this town that been really good. l.a. . yes, although i'm not personally feel like i feel like it's everybody's own choice, you know, because not everybody agrees with vaccines, but experts don't want people getting too excited. stressing that the manufacture and distribution of the vacc

s., if approved by the food and drug administration, it could be distributed by early or late december. the company said trials indicate their vaccine is 95 percent effective. and there's hope from other drugs firms. the u.s. drugs maker is also expected to apply for emergency approval. this week the company said its vaccine is 95 percent effective in trials astra zeneca oxford university plan to release results of very late stage trials before christmas. and russia says its sputnik 5 vaccine is 92 percent effective. the w.h.o. is in talks with moscow over a potential application for emergency approval. and that was the day after the conversation continues online after a good thing to the point is a strong opinion, a clear position on some international perspective. such research is a revolt. if it can breakthroughs in efforts to develop a vaccine against covert nineteen's, could this be the beginning of the end for the coronavirus night massacre and who showed up and will profit 1st find out to the point to the point that comes next to come to w. why are people forced to hide in truck

food and drug administration has issued emergency approval for a general wrong's antibody therapy. used to treat president trump. agency said the treatment should be used for mild to moderate cases of covert 19 troubles often in correctly described the therapy as a cure. earlier we spoke with a professor of epidemiology of medicine at columbia university. she says, the curfew alone isn't sufficient for tackling the rise and infections putting in place a curfew demonstrates the concern. certainly the concern by the governor of california . i think the curfew in of itself is not sufficient. i think it's one piece of the puzzle. i think it's important that curfew will hopefully decrease the numbers of people who congregate to gether. it will probably lead to more people staying at home, staying put, not travelling than meeting up with other people outside their home. so i think it will be of value certainly. but i think it needs to be combined with the other measures that we know work, for example, wearing masks all the time as well as congregating and socializing with people in one's

the antibody treatment has received emergency use authorization from the food and drug administration last week. i am hopeful it will help stop or at least slow dramatically the alarming rise of hospitalizations that we have seen across parts of my stage. so far, about 80000 doses are ready for distribution. we should have bet up to a million doses a day by the end of the year. while the quantity is limited at this point, every single dose could mean a life saved. this alone is cause for hope. butee the ghost good news does not stop there. last week pfizer announced covid-19 vaccine is more than 90% effective in clinical trials. thus this morning, mowed moderna had its vaccine candidate 95% effective. just an incredible result. this is exactly what we've invested billions of dollars in developing these life-saving drugs earlier this year. the funding we have appropriate is not only supported research and development but manufacturing of vaccine and therapeutics. we want to make sure distribution could begin as soon these drugs were approved as safe and effective. that is exactly the d

industry to, to have a foot in the door and this has definitely increased with the drug administration. and i'm pretty sure you and next us administration will stick to this goal for another district of the disputed nagorno-karabakh region that's been handed over to as a big. the last armenian soldiers left the area has part of a russia broken page still. but before troops abandoned their position, civilians had fled. the war zones of his more aghasi of tells the story of some of those made homeless by the conflict. everywhere you go, there is only desolation, despair, empty, burnt, and abandoned villages. rusty trucks palled with furniture, clothes, and who police souls. there's no one left but the awed desperate stragglers. it's so painful, unbearably painful, your entire life you have been billed in step by step, trying to make it a little more comfortable so you get something good. sound only a tool has just disappeared. gun lit, and her husband igor, for 17 years have made a hard living in the mountains raising cattle. when the barrow visited by john, the artillery became too much

decided by us industry to, to have a foot in the door and this has definitely increased with the drug administration. and i'm pretty sure what you and next us administration will stick to this goal. a reminder of our breaking news this hour the most regarded as perhaps the greatest.

>> reporter: we know that the food and drug administration has authorized regeneron for emergency use on those patients that have been determined to be high risk. it does not apply to patients that have been hospitalized and had to be potentially pout oxygen because of their treatment, to fight the virus. in terms of how soon people would potentially be treated with this drug, we do know that regeneron says that they are looking to have doses available for at least 80,000 patients by the end of this month. and potentially up to 200,000 patients by the start of the year. the u.s. food and drug administration on saturday issued an emergency use authorization for regeneron's antibody cocktail to treat covid-19 in high-risk patients with mild to moderate disease. president donald trump received the therapy when he was hospitalized for coronavirus. according to the fda, the cocktail, which mimics an immune response to infection, reduced covid-19-related hospitalizations and emergency room visits in some patients within 28 days of treatment. they t works best in patients who are given the t

if approved by the food and drug administration, it could be distributed by early or late december. the company said trials indicate their vaccine is 95 percent effective. and there's hope from other drugs firms. the u.s. drugs maker, is also expected to apply for emergency approval. this week the company said its vaccine is 95 percent effective in trials astra zeneca oxford university plan to release results of their late stage trials before christmas. and russia says its sputnik 5 vaccine is 92 percent effective. the w.h.o. is in talks with moscow over a potential application for emergency approval. and that was the day after the conversation continues on life after the w. i'm a good feeling to the point of strong opinions, clear positions of international perspective, submit researches are reporting. see difficult breakthroughs in efforts to develop a vaccine against covert 19. could this be the beginning of the end for the coronavirus nightmare, and who feel which one will profit 1st find out to the point short for the book. to the point that the beating the minutes on w., o. the

as the drug administration comes when, then those who dreams of a hoax ever be held accountable for media ever be held accountable for the game they play and should be. now, assuming it is truly welcome to staying connected has become more important than ever now that we're driven apart. how can you help us navigate the and charter waters of the post? i ask misha dollar professor in wireless communications at king's college london mission dollar professor in wireless communications and kids college london. great to have you with us. all right, so much to do 3 g. 4 g. . i mean, i don't remember any of them creating such a sensation as 5 g. networks and they say that 5 g. is truly a game changing set up in the quality of connection. why is it so, i mean, with that grates to speed and upwards to really be later before. why now, why, why such fuzz? yes, that is a good question you're raising and then it's, it's really, it's really curious to see of consumers will react really to the speed improvement of 5 g. . because you know, if we go on with a generation from 2 g. to 5 g. every time we imp

that means getting the thumbs up from the food and drug administration and considering the fact that the vaccine is relatively new and has not had the time to pass the usual scrutiny. pfizer and its german partner beyond tech are asking for emergency approval to get it out there fast. emergency use authorization or new way, isn't much different. standard only requires that a product may be a factor. and that f.d.a. performs an assessment in the emergency of the available data and sounds well, we think it's non-contentious benefits outweigh the non-contentious, the f.d.a. has emergency use of authorization is intended for public health emergencies. arguably, such as the corona virus, according to the us government approval of the vaccine, is expected in the 1st half of december, and advance trial which involved 41000 people worldwide showed that the pfizer beyond tech vaccine protects 94 percent of adults over 65, with some reporting minor side effects, other stats showed as 90 percent effective. either way, a good place to be with the front runners in the copen 1000 vaccine race, suc

food and drug administration for emergency approval of a covert 19 vaccine. it comes after the companies posted promising results from advanced trial. it showed a 94 percent success rate in adults over $65.00 and the park 89 months. after the start of this project, we have a reading list to my new 5 children get approved 4 boxes of this. as you can see, definitely use something of a will redefine your interest. it will start the clock on a process that could see the vaccine approved for use in the u.s. by mid december. once approved, distribution will become the focus and there's a mixed response from americans as to whether or not they will get the shot. of course. yeah, probably soon as possible. and not really to say that i don't even take the, the flu shot myself just because i'm out means system that when really good. how a yes or no. and not personally i feel like i feel like it's everybody's own choice. you know? because not everybody agrees with vaccines, but experts don't want people getting too excited. stressing that the manufacture and distributio

so when could it actually get the food and drug administration's go ahead? they arrived early in the they apply today for an emergency use of the food and drug administration. what they're trying to do here now is to prove their findings all of their latest study and that is 94 percent of the vaccine is effective, preventing cope with 19 and even 100 percent is effective, preventing severe cases. so very promising data on the also because the scene doesn't have to be stored as cold as the pfizer bio and take alternative that was introduced a little earlier. now the next steps are that the f.d.a. will meet with its advisory committee on december 17th, where they will review this application on december 10th already for the pfizer bio and take vaccine. so we earlier than that, and they are expected to grant emergency use authorization for both. that seems just a little while after that. probably one or 2 days later. so we might look around december 20th. so when could we see the 1st vaccinations actually taking place in the u.s.? so according to any fall to th

food and drug administration has issued emergency approval for generals antibody therapy, which was used to treat president trump when he was ill with the virus. the agency said the treatment should be used for miles to moderate cases of covert 19. president trump as often in correctly described the 3rd as a cure all for our souther is a professor of epidemiology meds at columbia university. she joins us now live from new york via skype good to have you with us. once again, this antibody drug, is it going to make any difference in the fight against the corona virus in the u.s.? well, it will make some difference. i think obviously we have not head down sufficient number of treatments for people who come down with caught with 1000 and having this antibody, evident, or for a subset of people who have her go in 1000. those who have mild, moderate disease will of course be at least an option for some people who are fortunate enough to be able to get this medication as an epidemiologist. what do you make of california's restrictions? well, i think it tells us senate tells certainly the people

the us food and drug administration has approved emergency use of, or general covert 19 treatments. and the u.k. will be the 1st country to begin clinical trials for a new antibody treatment developed by astra zeneca. it's designed to treat people with a weakened immune system who can't be vaccinated. meanwhile, the british government has confirmed what most already know. it won't be a normal christmas this year, and that's mr. ritchie soon. arc says the doing what they can to help families get together. england is back in lockdown. and prime minister boris johnson is expected to outline his winter virus strategy. place on monday. with regard to christmas and i think frustrating as it is for all of us christmas is not going to be normal. but that said the prime minister. and i will also looking at ways to see how families can spend some time with each other over christmas period. obviously that's something that we would like to do. health authorities in the gaza strip say the recent rise in corona virus infections could overwhelm the medical system. there within a week, they warned

well, for the us it's up to the food and drug administration, the f.d.a. . so there they have different procedures and we will see when the green light, we come from the e.u. may 4th for europe. doesn't it? these it tool assessments do not necessarily need to be aligned. i would say at this stage we have on one hand the procurement procedures ongoing for the 1st pyramid of these potential fixings. but we should let me do their job. their job is something different than the procurement negotiations for sealing these contracts for these potential vaccines against all the banking. and let me ask you, mr. not just, you know, the news that we've been reporting the last couple of weeks has been based on these preliminary data release is about the trials for these vaccines. do you think that data? should it be made public as early as it is, or should that be something that waits for the but, you know, the regulatory agencies such as e m a or the f.d.a. . well, we need to see exactly you're making a very valid point. there is a difference between these press release

food and drug administration has approved the 1st covered 19 home testing kit. it provides results within 30 minutes. now for other stories making news around the world, thousands of pro-democracy demonstrators have gathered in the thai capital of bangkok as normally as votes on changes to the constitution. they want the prime minister to step down, as well as that reforms to curb the powers of thailand's, monica, tuesday's demonstrations or so escalation in violence, the release 55 people injured, congo has declared its most recent epidemic to be outed and 55 people died in the outbreak in early june in the north western province of the health of the world, health organization says widespread vaccination help to curb the disease present. trump has fired his top cyber security official, chris krebs, via twitter, the president cusins him of making an inaccurate statement. when he confirmed that the security of the november 30th election, mr. trump continues to make claims of election fraud, which has yet to provide that evidence. i was just 2 months left in offic

food and drug administration's vaccine advisory committee is expected to meet in early december shares and jumped nearly 5 percent on the news. and pfizer is by more than one percent. well, before christmas knowledge should be music to investors, ears, and advice, but joins us now. in frankfurt, and there's a how optimistic are investors here in europe, that a vaccine will come our way sooner than expected? well actually there was a lot of fixie in optimism already in the markets. we have seen a almost record at most likely a record rally for november when it comes to accurate to say in europe. so there is a lot of optimism and a lot of hope that the vaccine comes from earlier than expected by one actually also has to look at the reality. and that's what investors are now doing as well. they're kind of, it's a bit of a more of a sober approach now because clearly, even if they have a fast track to approve of the 1st japs could be out by early january. but they value in texas also saying that they most likely in the 1st round, can provide some 15000000 doses, which them would mean a vac

media that vaccinations could begin 2 days after it's approved by the food and drug administration, which is meeting between the 8th and 10th of december. but a modest government says protestors who sent fire to the country's congress building on saturday are guilty of terrorist acts. but a human rights watchdog said the police used excessive force against them. thousands of demonstrators had gathered in central guatemala city to protest government cuts to education and health care spending human rights groups, a better reason, did more than 300 demonstrators in the capital. minsk, thousands protested for the 16th. straight sunday, calling on president alexander to step down. the president of rigging elections in august was a 2nd wave of corona virus infections. grip europe. the pandemic is stretching health care systems to breaking point. ukraine's underfunded hospitals are struggling to keep up with a surge in patient numbers. amid the spike frontline medical workers are among those suffering most recently, i knew that i'd get sick eventually. when i got the news that i was infected, it

the food and drug administration is giving the green light to regeneron's antibody cocktail for some patients who test positive for covid-19. the fda says it is okay to give to high-risk patients with mild or moderate symptoms. president trump received the therapy when he was battling covid-19. the cocktail contains two antibodies produced in a lab. regeneron says it will have doses for 80,000 pashttients th month. >>> in the south bay, santa clara county is expanding testing because of the increase in covid-19 cases there. the fairgrounds will be expanded to accommodate 3,000 points a day, starting next week. expansion won't stop there. the goal is to make room for 5,000 appointments a day by mid-december. that facility will also be testing for the flu, while testing for covid-19 and anybody can get a flu shot. >> we also continue to have a -- our flu shot clinic and where people can come in and get a free flu shot, regardless of their immigration status. regardless of medical insurance. they can definitely come here and get a flu shot. >> the facility accepts drive-through, bike, w

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food and drug administration's vaccine advisory committee is expected to meet him in december. shares in biotech, jumped nearly 5 percent on the news, and pfizer is by more than one percent. let's bring in our correspondent in new york quarter on this. yes. is there an urgency in the u.s. for a vaccine to be approved as soon as possible, given how the pandemic is going? yeah, definitely. health officials calling the virus situation very dangerous. so i'm standing here in front of a public elementary school in brooklyn, and the city announced just today on wednesday that all public schools will close again starting to morrow thursday, and go fully back to remote learning new york with about 1100000 students. this is a biggest school district, i'm in the country and you can imagine that this is really not a lot of time for families of working families to make adjustments other than the school. so we also have more and more lockdown measures in the country and also federal aid is going to expire in many cases in the next couple of weeks until it's a, it's a pretty tough situation

the regulation of the food and drug administration is what allows any of us to go to a pharmacy and notnk about the medice we get, right? we assume that it will be safe andffective because it's actually required by regulation to be safend effective. and every dose is required by regulation to be identical to another dose in a bottle. and that's all governed by an elaborate architecture of regulations called cgmp. current good manufacturing practices. these are very detailed regulations. you know, but the oy thihing that stand between us and pharmaceutical disaster is the effects of manufacturing companies, which is often dubis, and effective regulation by the fda, whi is often inadequate. so you know, this is something that i think is importa for reader to understand, you know, what is governing the safety of theill that they're swallowing? and you know, judging from the reviews of thebook, that's something that bottle of lies will make you stop and think ab about. as an investitive journalist, i have lon felt compelled t find out the truth. it might be a sort of peonality trait. i hate

efficacy, we have two safe vaccines that could be authorized by the food and drug administration to be distributed within weeks. operation warp speed has vaccine in a fe number of ways. operation warp speed has delivered a safe vaccine in a number of ways. and ensure there are no delays in vaccine production. because of this work, by the end of december, we expect to have 40 million doses of these two vaccines available for distribution pending f.d.a. distribution and going to our most vulnerable americans. we have been laying the groundwork in administration for months. there are four major caps to get the manufactured product to americans safely in order to save lives. allocation, distribution, administration and ongoing monitoring and data work. we have led the groundwork for these and paid for the vaccines and worked to ensure that the administration costs will be covered by private insurers and the federal government through medicare and medicaid for the uninsured american. we procured supplies like needles and personal protective equipment and assembled into kits that we will pai

reporter: on his white board is one possible scenario, the all-important approval by the food and drug administration of the vaccine developed by pfizer, followed by approval of another by moderna. >> what is d-day? >> the day we deliver the first round of vaccine for pfizer. >> reporter: that's when it would start to get complicated, because if approved, the pfizer vaccine would require patients to receive two separate shots 21 days apart. >> we know it's a two-dose vaccine, so we want to ensure that we can manage the delivery of the first dose and ensure the delivery of the second dose while we simultaneously integrate new rounds of doses being delivered to the american people. >> reporter: on top of that, the pfizer vaccine, which could be ready next month, has to be kept very cold until it is used. >> minus 80 degrees celsius which is 94 degrees farnt height, very hold. >> reporter: paul is a west point graduate who retired from the army this summer and became a civilian deputy. >> we have to make sure we send the vaccine to the right places that had the capacity or the ability to do the dry ice

food and drug administration and the european union today. the company just released no data on its study showing that there vaccine is more than 94% effective at preventing covid- 19. and 100% effective at preventing severe cases of the coronavirus. moderna has gotten about $1 billion from u.s. government and has a deal right now to supply 100 million doses with the u.s. government having an option for another hundred million doses. so, well on their way to making this actually happened. next step though is the fda approval. pfizer has already applied for that as well. so, the fda is going to be talking with its advisory committees during the month of december's and people could be rolling up their sleeves by 2021. >>> looking live at the san jose airport, santa clara county is ratcheting up its rules to keep people safe. emily turner joins us live from the airport with the new restrictions for travelers returning home today. >> reporter: if you are headed in today or pretty much any time over the next month, you are now going to have to han

being as high as it is about as a drug administration comes one, then those who dreamed up and executed the russia gate hoax ever be held accountable when the media ever be held accountable for the role they play and should be. now assume the deep state is truly the law. police brutality is back in the spotlight. c.c.t.v. footage captures the moment for french police officers on the beat. a black man, the offices have since been suspended. neighborhood my screams, he called me and asked what's going on. i explain and attacks and he wanted to call the police, but it was the police. it's outrageous. a relative of a yemeni civilian allegedly killed in u.s. drone strike in yemen says he continues to live in fear that as a top german call rules, the plane can distance itself from american strikes conducted from an air base.

media that vaccinations could begin two days after it is approved by the food and drug administration, which is needed between eight and tenth of december. protesters in guatemala city have set fire to part of the country's congress building. amid a growing demonstrations against the president and legislature, the demonstrators are unhappy with their leaders for approving a budget cuts to education and healthcare spending. the people of turkey now faso have been voting in a presidential election that's been overshadowed by a rising jihadist threat. president rock cabaret is expected to win reelection though opposition? candidates have criticized his failure to contain the violence opposition parties have warned of massive fraud and threatens not to accept the results show if they hope, as a prime minister has given the leaders in the northern region of a seventy two hour also made them to surrender threatening an all out assault if they do not. the ethiopian military has also warned civilians to get out of the regional capital make a way before the deadline. commanders say they will s

the food and drug administration is the gold standard in the world for regulating pharmaceuticals, they how to take a close eye and make sure drugs are safe and effective in the corona vaccine has been developed under more scrutiny than any other drug development process in history, there will be a public meeting next month at fda in the opening days of december whether they will review all the data, the public will have an opportunity to question scientist that have not been involved in the development it'll have an opportunity to take a close look at all this help fda make an informed and transparent decision. arthel: pfizer plans to distribute 50 million doses of vaccine to the end of this year which is like in the next five weeks and 1.3 billion doses next year. might we be in the most vulnerable. while we wait for the vaccine to make it to market? >> we can see light at the end of the tunnel but we're certainly not at the end of the tunnel yet, we have quite a ways to go. the american public may not appreciate this, to date there have been 770 drug development programs embarked on

food and drug administration has issued an emergency approval for general ones. antibody therapy. police of 4 with antigovernment protesters in guatemala, after hundreds stormed the congress building back and such. don't fire officers fired tear gas to clear the demonstration. ultra violent as widespread anger. the new budget which protesters say disenfranchise is poor and indigenous people go on . t.v. is a director at the freedom, a developing foundation in guatemala city. he says protests to see the budgets as benefiting politicians. the people the budget was destroyed or broke. the camel's back thing is that people were upset that the government mostly because to read it and then make their government back in march raised money that he was supposed to be for economic aid. but the aid never made it to the people who need it. the most so that's the main concern of people and now the congress approves these budget deal. you know, a very unusual wait they, they did it during night, you know, emergency session. and that was me, people in one of my love very, very upset. the thing i

food and drug administration has approved the 1st coated 1000 home testing kit. it provides results within 30 minutes. south australia has imposed a 6 day lockdown after a sudden outbreak end of a long period with no new infections. and japan has seen its biggest rise in new delhi cases as preparations begin for next summer's olympic games are, let's take a look now at some of the stories that are making headlines around the world. thousands have been marching through central warsaw, protesting moves to tighten poland's abortion law. it's the latest in a series of demonstrations. last month, the court handed down a ruling that would impose a near total ban on abortion. that ruling has yet to go into effect. thousands of anti-government protesters gathered in the thai capital bangkok as lawmakers rejected their demands for sweeping changes to the constitution. demonstrators want the prime minister to step down and they want curbs on the power of the monarchy. chaotic protests just a day earlier, left, more than 50 people injured. u.s. secretary of state my pump a.

so when the food and drug administration meets on december 8th, 9th and 10th, they said they'll not approve covid vaccine without a public meeting so everyone can see the data and have confidence. when they meet, we need to make sure we can distribute and administer the vaccine as smoothly as possible through january, through february without any slip-ups in the transition. so we need that cooperation right now. >> yes. yer yes, indeed. dr. michelle meeth, thank you. >> thank you. >>> what ivanka's latest tweet says about the investigation into her business. but everything fits in. still hard work. just a little easier. still a legend. just more legendary. chevrolet. making life's journey, just better. chevrolet. it's time you make the rules. so join the 2 million people who have switched to xfinity mobile. you can choose from the latest phones or bring your own device and choose the amount of data that's right for you to save even more. and you'll get 5g at no extra cost. all on the most reliable network. so choose a data option that's right for you. get 5g included and save up to $400 dol

pfizer plans to ask the food and drug administration for emergency authorization of the two dose vaccine it's seen no serious safety and health concerns. it also initially plans to have enough vaccine to immunize 15 million to 20 million people. >>> a live look at the big board for you this morning where we could see the dow is up more than 1,100 points right now. investors excited over the report of pfizer's covid-19 vaccine. over 90% effective. >>> let's take a peek outside this morning. the sun is coming up. is it really warming things up across the bay area? it would be nice. it's been near freezing in some spots out there. a really chilly start to our week and that cold weather may be hitting some businesses especially hard. let's check in with "today in the bay's" kris sanchez. these restaurants need people to come out but they'd better bundle up. >> reporter: they're, they're doing what they can to convince customers to continue buying into the outdoor experience even as the weather starts to turn a little bit colder. restaurants we talked with a adding heaters if they can find th