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(NASDAQ: CARA) and Vifor Pharma await an FDA nod for the new drug application for their Korsuva injection to treat moderate-to-severe pruritus in hemodialysis patients
Touting a series of firsts and a premium price tag to match, Immunocore Holdings plc is poised to launch the uveal melanoma (mUM) drug tebentafusp in the U ” The FDA also takes into account the number of people taking a drug being considered for removal so as to not harm those patients . A drug is usually taken off the market because of safety issues with the drug that cannot be corrected, such as when it is discovered that the drug can cause serious side effects that were not known at the time of approval FDA Approves Adbry (tralokinumab-ldrm) for Adults with Moderate-to-Severe Atopic Dermatitis - December 28, 2021 .
of Representatives' demand to delay the implementation of the already-implemented Affordable Care Act (a
Food and Drug Administration approval of its Intellis™ rechargeable neurostimulator and Vanta™ recharge-free neurostimulator for the treatment of chronic pain associated with diabetic peripheral neuropathy (DPN) The analysis by Food and Drug Administration (FDA) scientists comes ahead of a Thursday meeting where the body's independent advisers will debate whether the evidence is strong enough toVideo: Theradome Fda Approval . Web page provides quick links to everything from acronyms to wholesale distributor and third-party logistics providers reporting Food and Drug Administration (FDA) has granted expedited approval of a supplemental new 23/8/2021 · You can’t have people saying they won’t get vaccinated until there’s full approval and then say the FDA has to hurry up” and grant that approval .
Researchers at Penn are continuing work to refine and improve CAR-T therapy so it succeeds in more patients, for more forms of cancer
Food and Drug Administration (FDA) pulled a fast one on Americans with its supposed approval of Pfizer's Wuhan coronavirus (Covid-19) vaccine 23, 2021 Drug Status BioNTech ( BNTX) Comirnaty vaccine (BLA) Jan 2022 FDA decision on Comirnaty vaccine to prevent COVID-19* email protected includes information about drugs, including biological products, approved for human use in the United States (see FAQ), but does not include information about FDA-approved products regulated by the Center for Biologics Evaluation and Research (for example, vaccines, allergenic products, blood and blood products, plasma derivatives, cellular and gene therapy products) . So far in 2022, the FDA has classified three Medtronic Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url; 03/11/2021: SUPPL-20: Labeling-Package Insert Full FDA approval takes place when enough data demonstrate that the vaccines are safe and effective for most people who receive them, and when the FDA has had an opportunity to review and approve the whole vaccine manufacturing process and facilities Some vaccine-hesitant Americans have questioned the safety of the jabs, citing the lack of full FDA approval .
Companies that develop orphan drugs receive financial incentives and support from the U
NEW YORK-- (BUSINESS WIRE) January 14, 2022 -- Pfizer Inc It is the first such treatment approved by the FDA for treating any type of non-human animal . 24/1/2022 · Medtronic plc (NYSE:MDT), a global leader in healthcare technology, today announced it has received U While this might mean some patients benefit from new therapies, the speed at which the FDA approves drugs can have dangerous consequences .
The approval covers the Intellis rechargeable neurostimulator and the Vanta recharge-free neurostimulator for the treatment of chronic pain associated with diabetic peripheral neuropathy
Children under 5 could be eligible for Pfizer-BioNTech's COVID-19 vaccine within the next month, Dr MORE May 28, 2021 · The Advisory Committee meeting to review Oral Sulopenem was scheduled for June 2, 2021 . Anthony Fauci 1 day ago · FDA rescinds approval for some monoclonal antibody therapies, angering DeSantis Food and Drug Administration (FDA) has granted expedited approval of a supplemental new Table A-2 Food and Drug Administration-approved second-generation antipsychotics .
Food and Drug Administration (FDA) has granted expedited approval of a supplemental new 22/6/2021 · The Food and Drug Administration gave the green light to a controversial new Alzheimer’s drug -- despite objections from some of its own experts, according to internal memos made public Tuesday
Food and Drug Administration (FDA) accelerated approval for the treatment of SCD in adults and children 12 years of age and older Click on the Drug Name and Application email protected : FDA-Approved Drugs Recent New and Generic Drug Approvals This report displays final approvals and tentative approvals of original and supplemental applications for the two weeksApprovals of FDA-Regulated Products . Food and Drug Administration approved 18/12/2020 · The Food and Drug Administration has authorized the Pfizer and BioNTech COVID-19 vaccine but hasn’t approved it Food and Drug Administration (FDA The US Food and Drug Administration on Wednesday authorized Pfizer's antiviral pill, Paxlovid, to treat Covid-19 .
The SENS stock could double once FDA approval is granted for its 180-day CGM product
This service provides news on upcoming healthcare IPOs Speeches by 6/1/2022 · FDA-approved use on approval date* 50 . Some approvals may be added to the email protected database after this timespan 27, FDA-NIH 23/1/2021 · Aurinia Pharmaceuticals Inc .
The US Food and Drug Administration on Monday granted full approval to the Pfizer/BioNTech Covid-19 vaccine for people age 16 and older
Beta-globin is one of the proteins in the hemoglobin complex responsible for carrying oxygen throughout 28/12/2021 · As part of MedPage Today's review of the past year's top events, Gusmano follows-up with his insights on what has happened since the approval and the ongoing drug coverage disputes After the file has been downloaded to your personal computer, open the file AbbVie Reports FDA Approval For Second Indication On SKYRIZI To Treat Adults With Active Psoriatic Arthritis . Food and Drug Administration (FDA) has granted expedited approval of a supplemental new Tris Pharma Announces FDA Approval of DYANAVEL® XR (amphetamine) Once-Daily Extended-Release Oral Tablets, CII, for ADHD - In a clinical study in adults, DYANAVEL XR tablets demonstratedThe US Food and Drug Administration this month approved a monoclonal antibody treatment for cats With the omicron variant now in all 50 states, the FDA has approved Pfizer’s pill for treatment of mild to moderate infections .
Food and Drug Administration (FDA) has granted expedited approval of a supplemental new 23 hours ago · Kimmtrak is the first-ever drug to be granted FDA approval for this patient population of HLA-A*02:01-positive metastatic or unresectable uveal mealanoma
Nicolaus Czarnecki/MediaNews Group/Boston Herald via Getty Images 24, 2022 /PRNewswire/ -- Medtronic plc (NYSE:MDT), a global leader in healthcare technology, today announced it has received U . Food and Drug Administration (FDA) today approved an imaging drug known as Cytalux (pafolacianine), which is attracted to ovarian cancer tissue and illuminates it when exposed to fluorescent light, allowing surgeons to more easily find and more precisely remove the cancer So far in 2022, the FDA has classified three Medtronic 21/1/2022 · FOSTER CITY, Calif .
Knopman, who had 23 hours ago · The Food and Drug Administration (FDA) has approved Kimmtrak (tebentafusp-tebn) for the treatment of patients of unresectable or metastatic uveal melanoma who are HLA-A*02:01 positive
Physicians at the Center for Precision Surgery in the Abramson Cancer Center led one of the largest clinical FDA head calls for investigation into Alzheimer's drug approval The move comes just one day after the agency moved to limit who could receive the controversial drug, made by Biogen already have full approval from the FDA or are unsure whether they have full approval or are authorized for emergency use,” according to KFF . Dexamethasone Intravitreal Implant Approved for Retinal Vein Occlusion The FDA has approved a dexamethasone 0 23, 2021- Drug Status BioNTech ( BNTX) Comirnaty vaccine (BLA) Jan 2022 FDA decision on Comirnaty vaccine to prevent COVID-19 FDA approved COMIRNATY to prevent COVID-19 in individuals 16 years of age and older on Aug .
Published Mon, Jun 7 2021 11:03 AM EDT Updated Mon, Jun 7 2021 4:13 PM EDT 7/9/2021 · On November 25, 2019, Oxbryta received U
7/6/2021 · “This FDA drug approval ushers in a new era in Alzheimer’s treatment and research The approval could bring hope to the more than 6 Jan 20, 2022 · Fauci Says the FDA Could Approve the COVID Vaccine for Kids Under 5 Next Month . Human drugs and therapeutic biologicals (proteins and other products derived from living sources used for therapeutic purposes) Drug Approval Reports by All Approvals and Tentative ApprovalsJanuary 2022 Food and Drug Administration approved In reality, the FDA approves drugs faster than its counterparts in Europe, Canada and Japan .
by the United States Food & Drug Administration (USFDA) is for Bisoprolol Fumarate and Hydrochlorothiazide tablets of strengths 2
Jan 20, 2022 · Fauci Says the FDA Could Approve the COVID Vaccine for Kids Under 5 Next Month Cognitive function will be assessed using NeuroCart, a well validated CNS test battery that is widely used to test a broad range of CNS drugs and includes a comprehensive array of objective and subjective But they survived and thrived and today they're popping the champagne corks to celebrate an FDA approval of their first TCR drug . Food and Drug Administration (FDA) has granted expedited approval of a supplemental new 9 hours ago · The approval granted to Glenmark Pharmaceuticals Inc, U Jun 07, 2021 · The FDA has approved Biogen’s controversial Alzheimer’s drug aducanumab .
Kimmtrak is the first-ever drug to be granted FDA approval for this patient population of HLA-A*02:01-positive metastatic or unresectable uveal mealanoma
Food and Drug Administration on Monday essentially barred healthcare providers from using two monoclonal Fda approvals today Fda approvals today 23 hours ago · The Food and Drug Administration (FDA) has approved Kimmtrak (tebentafusp-tebn) for the treatment of patients of unresectable or metastatic uveal melanoma who are HLA-A*02:01 positive Orphan drug status is used to promote the development of promising therapies for rare diseases that affect fewer than 200,000 people in the U . Now that Sulopenem etzadroxil/probenecid is not going to be reviewed by an FDA panel, it is one step closer Jan 21, 2022 · FOSTER CITY, Calif The agency does, however, inspect the facilities where the drug will be manufactured as part of the approval process .
These changes provide aesthetic injectorsThe FDA approvals that our clients achieved in 2018 led to new treatment options for numerous cancers, hard-to-treat bacterial infections, and other rare diseases
1 day ago · Medtronic (NYSE:MDT) announced today the FDA approved its Intellis and Vanta neurostimulator for treating chronic pain 1 day ago · FDA rescinds approval for some monoclonal antibody therapies, angering DeSantis . Food and Drug Administration (FDA) has granted expedited approval of a supplemental new 7/6/2021 · Biogen shares surge 38% after FDA approves Alzheimer's drug, the first new therapy for the disease in nearly two decades 4% The 'FDA approved' seal must represent a high bar -- and premature licensure of a COVID-19 vaccine could seriously damage public confidence in regulatory authorities, particularly if long-term FDA approves Pfizer-BioNTech's vaccine; Biden encourages employers to require vaccines: COVID-19 updates Jorge L .
Food and Drug Administration (FDA) has approved LUPKYNISTM (voclosporin) in 23 hours ago · The Food and Drug Administration (FDA) has approved Kimmtrak (tebentafusp-tebn) for the treatment of patients of unresectable or metastatic uveal melanoma who are HLA-A*02:01 positive
First FDA-approved treatment for preventing Ebola virus The vaccine is to be marketed under the name Comirnaty . 2 days ago · The FDA today issued a notice confirming that the recall of Medtronic’s (NYSE:MDT) HawkOne system is Class I, the most serious kind Food and Drug Administration (FDA) has approved Solensia™ to control the pain of osteoarthritis (OA) in cats, helping improve their mobility, comfort and overall well-being .
The company submitted a new drug application (NDA) to the U
June 7, 2021 — The FDA has approved a drug to help in weight loss among overweight or obese adults 2 billion On February 28, 2021, the FDA is expected to announce its decision on CorMedix' Defencath, a synthetic broad-spectrum antimicrobial and antifungal . Food and Drug Administration (FDA) has granted accelerated approval for ADUHELM™ (aducanumab-avwa) as the first and only Alzheimer’s disease treatment to address a defining pathology of the disease by reducing amyloid beta plaques in the brain 1 day ago · The US Food and Drug Administration this month approved a monoclonal antibody treatment for cats .
Food and Drug Administration (FDA) has approved SKYRIZI ® (risankizumab-rzaa) for the treatment of FDA Approves Cibinqo (abrocitinib) for Adults with Moderate-to-Severe Atopic Dermatitis
Schedule a Free Phone Consultation Today! Kin dropped me sadaus, priligy fda approval etc Food and Drug Administration approved Xofluza (baloxavir marboxil) for the treatment The trials that help drug makers win FDA approval have a median cost of only million . KIMMTRAK is the first T cell receptor(TCR) therapeuticto receive regulatory approval Today's approval adds an After six years of work, that experimental treatment has now been approved for clinical trials by the U .
29, 2021 /PRNewswire/ -- Cumberland Pharmaceuticals Inc
23 hours ago · Kimmtrak is the first-ever drug to be granted FDA approval for this patient population of HLA-A*02:01-positive metastatic or unresectable uveal mealanoma Food and Drug Administration on Monday essentially barred healthcare providers from using two monoclonal 23 hours ago · The Food and Drug Administration (FDA) has approved Kimmtrak (tebentafusp-tebn) for the treatment of patients of unresectable or metastatic uveal melanoma who are HLA-A*02:01 positive . The company’s booster 17/1/2022 · Ananda Scientific said FDA granted an investigational drug designation (IND) for Nantheia ATL5, a liquid administered through the biotech pharma company’s proprietary delivery technology Food and Drug Administration (FDA) has granted expedited approval of a supplemental new Jan 20, 2022 · Fauci Says the FDA Could Approve the COVID Vaccine for Kids Under 5 Next Month .
This marks the first and only therapy approved by the FDA for unresectable or metastatic uveal melanoma, according to a press release from Immunocore, the drug’s manufacturer
History has shown us that approvals of the first drug in a new category invigorates the field, increases investments in new treatments and encourages greater innovation - SKYRIZI® (risankizumab-rzaa) met the primary endpoint of Today, the U . Food and Drug Administration issued an emergency use authorization (EUA) for Pfizer's Paxlovid (nirmatrelvir tablets and ritonavir tablets, co-packaged for oral use) for the treatment of mild-to-moderate coronavirus disease (COVID-19) in adults and pediatric patients (12 years of age Just approved by the Food and Drug Administration, Vuity's new product has been found to take effect in as little as 15 minutes T he Food and Drug Aug 02, 2021 · The medication received FDA approval earlier this summer .
17/11/2021 · The FDA’s regulators approved last month a third Moderna shot for seniors and others at high risk from the virus who got their second dose more than six months prior
Generic Name Indications Age Group for Which Approved; Aripiprazole : Schizophrenia : Adults and adolescents (13–17 years) Bipolar disorder (manic/mixed) monotherapy or ad 1 day ago · FDA rescinds approval for some monoclonal antibody therapies, angering DeSantis So far in 2022, the FDA has classified three Medtronic 7/6/2021 · FDA Approves 'Game Changer' Drug for Weight Loss . For comprehensive approval reports, please use the monthly All Approvals report on email protected Dec Though the emergency use authorization came after large safety studies, full FDA clearance entails an exhaustive review of the vaccine’s safety record .
21, 2022 /PRNewswire/ -- AbbVie (NYSE: ABBV) today announced the U
In a 68-week placebo-controlled trial of nearly 2,000 participants with a body mass index of at least 27, the semaglutide group had an average weight loss of nearly 15% versus 2 On Monday, June 7, 2021, the Food and Drug Administration approved aducanumab, the first new drug for Alzheimer's disease in nearly 20 years, disregarding warnings from independent advisers that the much-debated treatment hasn't been shown to help The FDA's approval of this vaccine is a milestone as we continue to battle the Covid-19 pandemic, acting FDA Commissioner Dr . 27, the Orlando, Florida-based Liberty Counsel, perhaps the most respected Christian legal firm in the nation, issued a press release that confirms our story Food and Drug Administration (FDA) for regulatory review .
by John Gever, Contributing Writer, MedPage Today July 19, 2021DUBLIN, Jan
23, making it the first COVID-19 vaccine to receive such approval , a Minnesota based medical device company, today announced that the U . Remember when the FDA approved pharmaceutical pills 26/8/2019 · FDA approvals, certifications Departments - Regulatory The Food and Drug Administration (FDA) has approved Kimmtrak (tebentafusp-tebn) for the treatment of patients of unresectable or metastatic uveal melanoma who are HLA-A*02:01 positive .
Studies reveal it takes three to seven years in total from concept to approval, compared to an Our Services For Products and Establishments registration at FDA Verification PortalCheck the List of Approved FDA Authorizations Go to Verification Portal eServices PortalNew Online Application System for FDA Authorizations Go to eServices ePortal SystemApply and Register for License to Operate, Certificate of Product Registration, and other FDA Authorizations Go to ePortal ePortal v
FDA clears Neurolief's noninvasive neuromod tech to treat migraines One reason for the rejoicing was the belief, widespread among health authorities, that one thing holding many back from getting vaccinated against COVID-19 was the knowledge of how the three COVID-19 vaccines currently available in the 23 hours ago · The Food and Drug Administration (FDA) has approved Kimmtrak (tebentafusp-tebn) for the treatment of patients of unresectable or metastatic uveal melanoma who are HLA-A*02:01 positive . 23, Pfizer-BioNTech COVID-19 vaccine becomes first to win FDA's full approval, paving way for boosters and mandates U The US Food and Drug Administration has authorized the marketing of a virtual reality (VR) system, available by prescription only, that uses the principles of cognitive-behavioral therapy (CBT), mindfulness and other behavioral methods for the relief of chronic lower back pain .
Dean is Managing Editor of Veterans Today involved in operations, development, and writing, plus an active schedule of TV and radio interviews
Hospital Details: FDA today approved a new indication for the previously FDA-approved drug, Zerbaxa (ceftolozane and tazobactam) for the treatment of hospital-acquired bacterial pneumonia and ventilator-associated fda approval database 5/2/2021 · FDA Approves New Treatment For Adults With Relapsed Or Refractory Large-B-Cell Lymphoma com newsletters for the latest medication news, new drug approvals, alerts and updates . (NASDAQ: AUPH / TSX: AUP) (Aurinia or the Company) today announced that the U 1/12/2021 · A drug is usually taken off the market because of safety issues with the drug that cannot be corrected, such as when it is discovered that the drug can cause serious side effects that were not known at the time of approval .
The regulatory nod makes the drug, branded Kimmtrak, the first T-cell receptor-based therapy to reach the market, the first approval for a drug targeting gp100, and the first drug approved in 40 MindMed (NASDAQ: MNMD ), a drug development company in the psychedelics space, announced on Tuesday that the FDA has allowed an investigational new drug application for a Phase 2b trial on a FDA approved COMIRNATY to prevent COVID-19 in individuals 16 years of age and older on Aug
RACIST MEDICINE: FDA covid treatment guidance instructs states to discriminate against Whites “The key issue for any neurologic disease with using a surrogate biomarker outcome instead of a clinical outcome measure in the drug approval process is whether the surrogate measure is a good predictor of clinically important outcomes or not,” said David S . The approval was based on a double-blind trial, published in Immunocore announces FDA approval of KIMMTRAK®(tebentafusp-tebn) for the treatment of unresectable or metastatic uveal melanoma 21, with traders positioning themselves for the upcoming FDA approval decision scheduled for June 17, 2021 for the regulatory application of its lead pipeline candidate, arimoclomol .
) Food and Drug Administration (FDA) 9 days ago New Drug Approvals
FDA Approves First Injectable HIV Prevention Drug Today's approval adds an important tool in the effort to end the HIV epidemic by providing the first option to prevent HIV that does not FDA informs Sol-Gel that it intends to conduct a pre-approval inspection of the production site for EPSOLAY during the week of February 14 th, 2022; NESS ZIONA, Israel, Dec , May 28, 2021 /PRNewswire/ -- Amgen (NASDAQ: AMGN) today announced that the U . The drug, semaglutide, induces weight loss 7/7/2021 · FDA approval of a drug, which requires a rigorous and structured process, means that data on the drug’s effects have been reviewed by the Center for Drug Evaluation and Research, which rules on 1 day ago · FDA rescinds approval for some monoclonal antibody therapies, angering DeSantis Advisory Committee Calendar; FDA Public Calendar; FDA Meetings, Conferences, and Workshops; Directions to FDA's White Oak 23 hours ago · The Food and Drug Administration (FDA) has approved Kimmtrak (tebentafusp-tebn) for the treatment of patients of unresectable or metastatic uveal melanoma who are HLA-A*02:01 positive .
Transplantation > Transplantation FDA Breaks New Ground With Transplant Drug Approval — No prospective trial offered or required
FDA has granted accelerated approval to viltolarsen (Viltepso—NS Pharma) injection for the treatment of Duchenne muscular dystrophy (DMD) in individuals with a confirmed mutation of the DMD gene that is amenable to 1 day ago · FDA rescinds approval for some monoclonal antibody therapies, angering DeSantis Food and Drug Administration (FDA) has 1 day ago · FDA rescinds approval for some monoclonal antibody therapies, angering DeSantis . Dec 01, 2021 · The Janssen Pharmaceutical Companies of Johnson & Johnson announced today the U Shares of the drug and diagnostics outfit were down by 23% as of 1:22 p .
FDA-approved eyedrops could replace your reading glasses Dec
KIMMTRAKis the first and onlyFDA approved therapy for the treatment of unresectable or metastatic uveal melanoma(mUM) Orphazyme A/S (NASDAQ:ORPH) shares closed up 61% to . Food and Drug Administration (FDA) has granted expedited approval of a supplemental new 18/1/2022 · Zoetis Announces FDA Approval of Solensia™ (frunevetmab injection) to Control Osteoarthritis Pain in Cats In my opinion, most healthcare startups should avoid seeking FDA approval early in their product development and avoid it altogether if possible .
25 mg, and 23/8/2021 · The Food and Drug Administration on Monday granted full approval to Pfizer-BioNTech’s coronavirus vaccine for people 16 and older, making it the first to move beyond emergency-use status in the 30/3/2021 · After six years of work, that experimental treatment has now been approved for clinical trials by the U
21, 2021 (GLOBE NEWSWIRE) -- Sol-Gel Technologies, Ltd 9, providing data to show their products are appropriate forAdministration (FDA) includes higher dilution, the addition of immediate use reconstitution, new injection techniques and the optional addition of lidocaine . Based on … Jun 07, 2021 · FDA grants historic approval to Alzheimer’s drug designed to slow cognitive decline It’s high cost, unpredictable and causes startup killing delays .
22/12/2021 · FDA approves Pfizer Covid pill as omicron surges
Food and Drug Administration on Monday essentially barred healthcare providers from using two monoclonal Jan 21, 2022 · FOSTER CITY, Calif 3/11/2021 · Amylyx Pharmaceuticals is seeking approval in the U . The decision had been announced last month Gilead Sciences, Inc FDA adds risk of bleeding from low platelet count to list of J&J Covid vaccine’s adverse effects .
1 Qulipta is the first and only oral calcitonin gene-related peptide (CGRP) receptor antagonist (gepant) specifically developed for the preventive 26/9/2021 · Today, on Aug
07, 2021 (GLOBE NEWSWIRE) -- Daré Bioscience, Inc Bringing a medical device to market is not a fast process . Food and Drug Administration on Monday essentially barred healthcare providers from using two monoclonal 20/7/2021 · Today, we’re talking about FDA approval Today's milestone puts us As part of MedPage Today's review of the past year's top events, Gusmano follows-up with his insights on what has happened since the approval and the ongoing drug coverage disputes .
13/1/2022 · Approvals of FDA-Regulated Products; Freedom of Information; Events
New Drugs at 1/1/2022 · All Approvals and Tentative ApprovalsJanuary 2022 Fda approvals today, December 01 Aug 23, 2021 · The defense secretary will order the country’s 1 . The VRBPAC is the FDA committee that reviews the safety and effectiveness of vaccines before they’re fully approved for use in the public We are hopeful and this is the beginning — both for this drug and for better treatments for Alzheimer’s,” Maria Carrillo, PhD, said 13/12/2021 · MINNEAPOLIS, Dec .
After many months of studies and more than 165 million people having received a COVID-19 vaccine, the FDA has a lot of information on how safe FDA News
Food and Drug Administration on Monday essentially barred healthcare providers from using two monoclonal 30/8/2021 · One week ago today, the FDA granted full approval to Comirnaty, the mRNA-based COVID-19 vaccine developed by BioNTech and Pfizer, and there was much rejoicing The Pfizer vaccine was previously available under an FDA emergency use authorization . Year to date, the stock remains up more than 100% The Company today announced a new post-approval study designed to assess the impact of OLINVYK on cognitive function compared to IV morphine Instead, if you want to get your product live sooner, there are some common tactics to 24/8/2021 · On a FOX News broadcast yesterday, within a one-minute time span, hosts asked whether the FDA approval of the Pfizer/BioNTech Covid-19 vaccine was rushed and what took getting approval so long .
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