The https:// ensures that you are connecting to the Today, the U.S. Food and Drug Administration approved the first COVID-19 vaccine, known as the Pfizer-BioNTech COVID-19 Vaccine, now marketed as Comirnaty (koe-mir'-na-tee), for the prevention of COVID-19 disease in individuals 16 years of age and older. Joint CDC and FDA Statement on Johnson & Johnson COVID-19 Vaccine. It is unclear how this will impact holdovers of requirements to be "fully vaccinated" from earlier in the pandemic, like for health care providers. Please enable it to take advantage of the complete set of features! The agency also is responsible for the safety and security of our nations food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products. (agenda), FDA Authorizes Changes to Simplify Use of Bivalent mRNA COVID-19 Vaccines. In this episode of omg OMx, Bruker's science-driven podcast, Kate Stumpo interviews Daniel Hornburg, the VP of Proteomics at Seer, as they discuss the innovative technologies in plasma proteomics. Recommendations for vaccine sponsors regarding the scientific data and information that would support the issuance of an emergency use authorization (EUA) for an investigational vaccine intended to prevent COVID-19. As of April 12, more than 6.8 million doses of the Johnson & Johnson (Janssen) vaccine have been administered in the U.S. CDC and FDA are reviewing data involving six reported U.S. cases of a. Health Canada issues label change on the AstraZeneca and COVISHIELD COVID-19 vaccines, Health Canada's COVID-19 vaccines and treatments portal. And most recently, the FDA suggested that manufacturers of ranitidine recall all lots and types of these medications. They help us to know which pages are the most and least popular and see how visitors move around the site. analyse site usage and support us in providing free open access scientific content. Over 900 million doses of the Moderna COVID-19 vaccine have been administered worldwide to date. If you do not allow these cookies we will not know when you have visited our site, and will not be able to monitor its performance. Before People should seek medical attention if they experience any persistent, new or worsening symptoms. Update: April 18th, 2021 05:17 EDT. Healthcare professionals should be alert to the signs and symptoms of thromboembolism and thrombocytopenia so that they can promptly treat these conditions according to availableevidence and clinical. Information on recalled lots of is available by year from FDAexternal icon. Other. Yesterday, the Janssen COVID-19 Vaccine Fact Sheet for Healthcare Providers Administering Vaccine (Vaccination Providers) was revised to include a Warning conveying that reports of adverse events following use of the vaccine under emergency use authorization suggest increased risks of myocarditis and pericarditis, particularly within the period 0 through 7 days following vaccination. 2022 Nov 23;11(1):39. doi: 10.1186/s13584-022-00548-3. The BCG vaccine does not decrease the risk of COVID-19 in healthcare workers. The drugmaker has recalled some doses of the vaccine in Europe after a "foreign body" was found in one vial. FDA Will Follow The Science On COVID-19 Vaccines For Young Children. The FDA expanded the emergency use authorization for the Pfizer-BioNTech COVID-19 Vaccine to include 12 15 year olds and issuedan updated FDA COVID-19 Response At-A-Glance Summary. The data accrued with the investigational bivalent Moderna COVID-19 vaccine (original and omicron BA.1) and with the monovalent Moderna COVID-19 Vaccine are relevant to the Moderna COVID-19 Vaccine, Bivalent because these vaccines are manufactured using the same process. Cookies used to make website functionality more relevant to you. Cookies used to track the effectiveness of CDC public health campaigns through clickthrough data. "We may have a variant that will come out, that will emerge over the summertime, that may become dominant, that might not be as well neutralized by whatever we pick," Marks said. or 3.4 million doses. "Although there was no vote at this meeting, ACIP members expressed their support for these recommendations," the CDC said in a statement. Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the third vaccine for the prevention of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Med Lett Drugs Ther. A Perspective on the FDAs COVID-19 Response. This is in line with the findings of other regulators. Since its initial publication, the scientific report has now been peer reviewed and accepted for publication in a Scientific Journal. The available data continue to demonstrate that vaccines prevent the most serious outcomes of COVID-19, which are severe illness, hospitalization, and death.. FDA Authorizes Updated (Bivalent) COVID-19 Vaccines for Children Down to 6 Months of Age. Following a thorough safety review, the U.S. Food and Drug Administration and the U.S. Centers for Disease Control and Prevention have determined that the recommended pause regarding the use of the Johnson & Johnson (Janssen) COVID-19 Vaccine in the U.S. should be lifted. Do ketogenic diets elevate low-density lipoprotein cholesterol levels? Joint Statement from HHS Public Health and Medical Experts on COVID-19 Booster Shots. Today, the FDA authorized the following uses of the Pfizer-BioNTech COVID-19 Vaccine, Bivalent for individuals 6 months through 4 years of age with certain types of immunocompromise who have previously received three 0.2 mL doses (Pfizer-BioNTech COVID-19 Vaccine or Pfizer-BioNTech COVID-19 Vaccine, Bivalent): Recombinant Protein-Based COVID-19 Vaccines Workshop(9:00 a.m. - 1:00 p.m. The FDA is integral in the fight against the coronavirus, using science and innovative approaches to take a broad range of actions that advance our nations response. Additionally, the FDA issued a report that describes some of the approaches used by the South Korean government to address COVID-19, particularly regarding development, authorization and use of diagnostic tests. The FDA took additional actions regarding booster doses of COVID-19 vaccines, including authorizing heterologous (or mix and match) booster doses in eligible individuals following completion of primary vaccination with a different available COVID-19 vaccine. The site is secure. Of the 78 million doses of the AstraZeneca and COVISHIELD vaccines that have been given in the Europe and the United Kingdom as of May 27, 2021, six cases of capillary leak syndrome were reported following immunization with these vaccines. The committee will meet in open session to discuss a request to amend Pfizer-BioNTechs Emergency Use Authorization (EUA) for administration of their COVID-19 mRNA vaccine to children 5 through 11 years of age. and transmitted securely. Your audience is not a, You need to speak in English when talking about the vaccine, please and. The FDA has been notified by Pfizer that new data have recently emerged regarding its emergency use authorization request for the use of the Pfizer-BioNTech COVID-19 Vaccine in children 6 months through 4 years of age. (a) Anterior chest wall treatment plan (Patient 2). Single-cell analyses also revealed an expansion of activated CD4+ T cells and robust spike-specific polyfunctional CD4 T cell responses following vaccination. Today, FDA announced that it has found certain lots of Astra Zeneca COVID-19 vaccine drug substance manufactured at the Emergent facility in Baltimore, Maryland, to be acceptable for use for potential export. Asked why the U.S. took longer to greenlight additional shots, Marks said the FDA needed additional time to complete "a very major action of consolidation" across all mRNA shots as well as to vet data on the second boosters. Read the press release and listen to themedia call. The most comprehensive solution to manage all your complex and ever-expanding tax and compliance needs. Rather, the manufacturers quality testing noticed some irregularity in some vaccine vials. In the late 1940s and early 1950s, before vaccines were available, polio outbreaks caused more than 15,000 cases of paralysis each year, with U.S. deaths peaking at 3,145 in 1952. FDA In Brief: FDA Authorizes Longer Time for Refrigerator Storage of Thawed Pfizer-BioNTech COVID-19 Vaccine Prior to Dilution, Making Vaccine More Widely Available. FDA Takes Multiple Actions to Expand Use of Pfizer-BioNTech COVID-19 Vaccine. The labeling changes for capillary leak syndrome were initiated after international reports of this very rare side effect were reviewed in Europe. (2023, February 22). Meta-analysis shows phytosterol-fortified foods effectively lower LDL cholesterol levels. Healthcare professionals should report any event potentially related to a vaccine. Health Canada has updated the product monographs (labels) for the Pfizer-BioNTech and Moderna COVID-19 vaccines to describe very rare reports of myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the tissue surrounding the heart) following vaccination.. Cases of myocarditis and/or pericarditis following immunization with COVID-19 vaccines have been reported . The committee will discuss the Emergency Use Authorization (EUA) of the ModernaTX Inc. COVID-19 vaccine and the Janssen Biotech Inc. COVID-19 vaccine for the administration of an additional dose, or booster dose, following completion of the primary series, to individuals 18 years of age and older. The country has become the world's most populous, but there are doubts about whether that title heralds a growth in wealth and influence. Report any adverse eventsafter immunization to your healthcare professional. Beware of Fraudulent Coronavirus Tests, Vaccines and Treatments. 2004;73:7980.85. FDA Issues Emergency Use Authorization for Third COVID-19 Vaccine. On April 14, the FDA issued an emergency use authorization (EUA) to InspectIR Systems for their InspectIR COVID-19 Breathalyzer test. CDC analyzed reports to theVaccine Adverse Event Reporting System (VAERS) to search for any side effects that might have been caused by the irregularity, and found none. Why would a vaccine, or certain batches of a vaccine, be withdrawn or recalled? FDA to Hold Advisory Committee Meetings to Discuss Emergency Use Authorization for Booster Doses and COVID-19 Vaccines for Younger Children. Sally first developed an interest in medical communications when she took on the role of Journal Development Editor for BioMed Central (BMC), after having graduated with a degree in biomedical science from Greenwich University. The team used single-cell RNA sequencing and functional assays to assess humoral (antibody) and cellular responses to two doses of either the Pfizer-BioNTech or Moderna mRNA vaccine (14 days following a second dose) in four individuals. The FDA is announcing two upcoming meetings of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) to discuss newly available data for the currently available COVID-19 vaccines. Robertson, Sally. People who were vaccinated with a vaccine from that lot might need to be vaccinated again to ensure they are protected against the disease. FDA's Dr. Janet Woodcock on COVID-19 Vaccines and Treatments. Centers for Disease Control and Prevention. The FDA amended the emergency use authorizations (EUAs) of the Moderna COVID-19 Vaccine, Bivalent and the Pfizer-BioNTech COVID-19 Vaccine, Bivalent to authorize their use as a single booster dose in younger age groups. Additionally, the agency will continue hosting virtual town halls for test developers for SARS-CoV-2 on July 27 and August 24 from 12:05 p.m. 1 p.m. FDA leaders participate in a virtual meeting with racial and ethnic minority community members about FDAs COVID-19 vaccine work. FDA Takes Key Action By Approving Second COVID-19 Vaccine. He added, "Evidence is now available that most of the U.S. population 5 years of age and older has antibodies to SARS-CoV-2, the virus that causes COVID-19, either from vaccination or infection . The FDA formally accepts Priority Review designation for the Biologics License Application (BLA) for their mRNA vaccine to prevent COVID-19 in individuals 16 years of age and older. Cases of these very rare events of blood clots associated with low levels of blood platelets following immunization with the AstraZeneca and COVISHIELD COVID-19 vaccines were first reported in Europe in early March. 2021 Nov 1;111(3):835-836. doi: 10.1016/j.ijrobp.2021.06.023. Accessibility NDMA has also been found in metformin, a diabetes drug taken by over 15.8 . View written testimony. Today, the FDA authorized a manufacturing change for the Moderna COVID-19 Vaccine to include an additional presentation of the vaccine for booster vaccination doses only. Covid-19 vaccine will likely require 2 doses The commissioner has the authority to allow unapproved medical products to be used in an emergency when there are no adequate or approved. FDA Expands Eligibility for Pfizer-BioNTech COVID-19 Vaccine Booster Dose to Children 5 through 11 Years. Would you like email updates of new search results? But older adults, ages 65 and older, can now get another bivalent shot as long as it has been at least four months after their last dose. See this image and copyright information in PMC. Viral vector-based vaccines. 2022 Nov-Dec;7(6):101048. doi: 10.1016/j.adro.2022.101048. RRP has been known to be triggered by a number of chemotherapy agents. The FDA amended the emergency use authorizations (EUAs) of the Moderna COVID-19 Vaccine and the Pfizer-BioNTech COVID-19 Vaccine to authorize bivalent formulations of the vaccines for use as a single booster dose at least two months following primary or booster vaccination. (b) Acute skin reaction after, MeSH Additional shots have already been cleared in some countries abroad. Today, the FDA added new devices to the device discontinuance list, including sterilization products and oxygen conservers. This article is terrible! The Law Did Not Treat Them Kindly. Reuters provides business, financial, national and international news to professionals via desktop terminals, the world's media organizations, industry events and directly to consumers. You can review and change the way we collect information below. The vaccine makers In a July 20, 2022, email, to lead Stories, Pfizer said this about the social media recall claim: The vaccine has not been recalled. Public health and medical experts from the U.S. Department of Health and Human Services released a statement on the Administrations plan for COVID-19 booster shots for the American people. For patients with cancer being treated with radiation with significant dose to skin, consideration should be given to the probability of RRP side effects from vaccinations against COVID-19. Learn why you and your loved ones should get vaccinated and boosted when eligible. FDA is committed to making decisions regarding the authorization or approval of COVID-19 vaccines that are guided by science and data. Japanese authorities last year suspended the use of some doses of the vaccine, which Moderna later recalled, after an investigation found stainless steel contaminants in some vials. Dr. Stephen Hahn explains the FDAs role in ensuring safety, effectiveness of COVID-19 vaccines. Radiation Recall Phenomenon Following COVID-19 Vaccination. If you got the J&J vaccine, the CDC recommends that if you are age 5 years or older, that you receive one. Researchers in the United States have conducted a study showing that the coronavirus disease 2019 (COVID-19) vaccines developed by Pfizer-BioNTech and Moderna generate a coordinated. The FDA announced approved COMIRNATY (COVID-19 Vaccine, mRNA) for active immunization to prevent COVID-19 in individuals 12 through 15 years of age. In this 30-minute video discussion, FDA Commissioner Dr. Stephen Hahn and Center for Biologics Evaluation and Research (CBER) Director Dr. Peter Marks talk with WebMD about what we know, what we don't know, and what we might learn in the futureabout COVID-19 vaccines. From nanoparticle-based enrichment to mass spec refinements, they explore how these tools facilitate unbiased, deep, and rapid proteomics. News-Medical. The Moderna COVID-19 vaccine label already contains safety information . Cookies used to enable you to share pages and content that you find interesting on CDC.gov through third party social networking and other websites. The FDA placed all alcohol-based hand sanitizers from Mexico on a country-wide import alert; issued warning letters jointly with the Federal Trade Commission to two companies selling unapproved products with fraudulent COVID-19 claims; and updated the COVID-19 frequently asked questions (FAQ). Health Canada recommends that people with a history of capillary leak syndrome not be vaccinated with the AstraZeneca or COVISHIELD COVID-19 vaccine. The United Kingdom began offering second doses of bivalent vaccine this month to some vulnerable residents, like those 75 and older. When a recall is related to a possible safety concern noted by the manufacturer, people who were vaccinated should be aware of their reaction to the vaccine, and talk to their doctor if they have any concerns that they may be having a reaction. Healthcare professionals are being advised that, while specific risk factors for this condition have not yet been identified, the benefits and risks of vaccination with these vaccines should be considered in patients with previous history of thrombosis, as well as patients with autoimmune disorders (including immune thrombocytopenia). Its safety and effectiveness in people younger than 6 months have not yet been established. All quotes delayed a minimum of 15 minutes. No, the Moderna COVID-19 vaccine was not recalled in the United States. By clicking "Allow All" you agree to the storing of cookies on your device to enhance site navigation, Study shows no significant cognitive benefit of adhering to Mediterranean diets regardless of calorie intake. View October 14 livestream. . No. FDA Offers Guidance to Enhance Diversity in Clinical Trials, Encourage Inclusivity in Medical Product Development. 2 killed, 4 wounded in Mississippi shooting; man arrested, 150 years later, Dixon bridge tragedy among nation's worst, Presidential candidate Vivek Ramaswamy says he wants to 'shut down the FBI' and replace it with something that sounds a lot like the FBI, Sanders: Biden could win in a landslide, Videos appear to show the aftermath of a precision strike by US-supplied HIMARS missiles on officers' quarters at a Russian base in Ukraine, Met Gala 2023 live updates: Get set for fashion's big night, Mizzous Isaiah McGuire selected in 2023 NFL Draft. Young children who were never vaccinated before would still need two doses of Moderna or three doses of Pfizer-BioNTech for their initial shots. (a) Posterior chest wall treatment plan (Patient 1). Statement by FDA Commissioner Stephen M. Hahn, M.D. FDAsCenter for Biologics Evaluation and Research (CBER)regulates vaccines and other biological products. In mid-July, the FDA held a stakeholder call to discuss COVID-19 vaccines, including preliminary reports of Guillain-Barr Syndrome following Janssen (Johnson & Johnson) COVID-19 vaccination. AS English. Cutis. Canadian health officials said during a press conference Monday the specific syndrome is being called Vaccine-Induced Prothrombotic Immune Thrombocytopenia (VIPIT) and that they are in contact. The site is secure. The FDA authorized a second booster dose of either the Pfizer-BioNTech or the Moderna COVID-19 vaccines for older people and certain immunocompromised individuals. April 18, 2023: FDA authorizes changes to simplify use of bivalent mRNA COVID-19 vaccines. The Vaccines and Related Biological Products Advisory Committee will meet in open session to discuss Emergency Use Authorization (EUA) of the Moderna Inc. COVID-19 Vaccine for the prevention of COVID-19 in individuals 18 years and older. The FDA updated the Pfizer-BioNTech emergency use authorization (EUA) to support the extension of shelf-life of the Pfizer-BioNTech COVID-19 Vaccine stored at -90 degrees to -60 degrees Celsius from 6 months to 9 months. and Director, FDA Center for Biologics Evaluation and Research, Peter Marks, M.D., Ph.D., discuss the Pfizer-BioNTech COVID-19 Vaccine booster dose. Listen to media call. The .gov means its official.Federal government websites often end in .gov or .mil. Your audience is not a meeting of the virology symposium of America. "At this stage of the pandemic, data support simplifying the use of the authorized mRNA bivalent COVID-19 vaccines and the agency believes that this approach will help encourage future vaccination," the FDA's top vaccines official Dr. Peter Marks said in a release Tuesday announcing their authorization. Before sharing sensitive information, make sure you're on a federal government site. As a result, the Department has updated warnings on the label for the AstraZeneca COVID-19 vaccine and COVISHIELD vaccine to inform Canadians and healthcare professions of these possible side effects and to provide information about the signs and symptoms and when to seek prompt medical attention following vaccination. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. The original "monovalent" versions of Moderna and Pfizer COVID vaccines are no longer recommended or authorized for emergency use in the United States after the Food and Drug Administration. Unable to load your collection due to an error, Unable to load your delegates due to an error. National Library of Medicine While typical COVID-19 vaccine side effects like a sore arm, mild fever, body aches or a dull headache aren't cause for alarm, if you've recently had the Johnson & Johnson vaccine and. This news article was a review of a preliminary scientific report that had not undergone peer-review at the time of publication. neurological symptoms, such as severe and persistent worsening headaches or blurred vision. Please use one of the following formats to cite this article in your essay, paper or report: Robertson, Sally. FDA Limits Use of Janssen COVID-19 Vaccine to Certain Individuals. Is there an association between COVID-19 and the risk of developing an autoimmune disease? To highlight how far the field of genetics has come, we spoke with Dr. Francis Collins, the leader of the Human Genome Project about his incredible career in genetics. Most requested. FDA announced a virtual meeting of its Vaccines and Related Biological Products Advisory Committee on Feb. 15 to discuss the request for emergency use authorization of the Pfizer-BioNTech COVID-19 Vaccine for use in children 6 months through 4 years of age. The .gov means its official. Todays authorizations follow discussions that occurred during a meeting with the FDAs Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Jan. 26. As the public health agency responsible for regulating medical products, we must ensure that health care providers have the most up-to-date diagnostics, treatments and vaccines in their toolbox to fight this pandemic. Update: The FDA updated this safety communication to clarify that the ACON Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing) in dark blue packaging is a product of ACON Biotech (Hangzhou) Co., Ltd. FDA Postpones Advisory Committee Meeting to Discuss Request for Authorization of Pfizer-BioNTech COVID-19 Vaccine for Children 6 Months Through 4 Years of Age. The FDA amended the emergency use authorizations (EUA) for both the Moderna and Pfizer-BioNTech COVID-19 vaccines authorizing use of a single booster dose for all individuals 18 years of age and older after completion of primary vaccination with any FDA-authorized or approved COVID-19 vaccine. You would most likely hear from your doctor if a vaccine given to you or your child is recalled. 2010;15:12271237. Unvaccinated adults will still also be able to elect to get their initial shots from the original Novavax or Johnson & Johnson supplies for now, although the CDC warned jurisdictions earlier this year that all remaining stocks of Johnson & Johnson's vaccine are set to expire next month. The American public puts its trust in the agency to ensure that all medical products, including COVID-19 vaccines, meet the agencys standards for quality, safety and effectiveness. The CDC's decision came after an hours-long meeting of the agency's outside advisers, the Advisory Committee on Immunization Practices (ACIP), to discuss the FDA's changes. HHS Vulnerability Disclosure, Help The viral spike protein mediates the initial stage of the SARS-CoV-2 infection process and is the primary target of antibodies following natural infection or vaccination. WHAT WE FOUND Int J Radiat Oncol Biol Phys. Issue: Health Canada is updating the AstraZeneca and COVISHIELD COVID-19 vaccine labelling information as it continues its safety review regarding very rare events of blood clots associated with low levels of platelets following immunization. Bethesda, MD 20894, Web Policies -, Garza L.A., Yoo E.K., Junkins-Hopkins J.M., et al. If you have received the AstraZeneca or COVISHIELD COVID-19 vaccine: Seek prompt medical attention immediately if you have any of the following symptoms four or more days after vaccination: If you experienced rare blood clots with unusual platelets following your first dose of the AstraZeneca or COVISHIELD COVID-19 vaccine, it is not recommended that you receive a second dose of any version of the AstraZeneca vaccine. On March 24, Health Canada updated the product monograph-or label-for the AstraZeneca and COVISHIELD COVID-19 vaccines to provide information on very rare reports of blood clots associated with low levels of blood platelets following immunization with the AstraZeneca vaccine. FDA Insight: Vaccines for COVID-19, Part 1. These cookies allow us to count visits and traffic sources so we can measure and improve the performance of our site. News-Medical, viewed 01 May 2023, https://www.news-medical.net/news/20210718/Pfizer-BioNTech-and-Moderna-COVID-19-vaccines-establish-recall-responses-to-reinfection.aspx. Curr Dermatol Rep. 2022;11(4):252-262. doi: 10.1007/s13671-022-00374-5. (Reuters) -Moderna Inc said on Friday it was recalling 764,900 doses of its COVID-19 vaccine made by its contract manufacturer Rovi after a vial was found contaminated by a foreign body. The specter of particulates has forced another recallthis time on Moderna's massively successful COVID-19 vaccine Spikevaxand the latest pull isn't contract manufacturer Rovi's first . Robertson, Sally. Over 900 million doses of the Moderna COVID-19 vaccine have been administered worldwide to date. Vaccine Adverse Event Reporting System (VAERS), How Vaccines are Tested, Licensed, and Monitored for Safety, FDAs Recalls, Withdrawals, Field Corrections, & Notifications, Centers for Disease Control and Prevention, National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Division of Healthcare Quality Promotion (DHQP), Diphtheria, Tetanus, and Pertussis Vaccines, Measles, Mumps, Rubella, Varicella (MMRV) Vaccines, CDC Statement: 2004 Pediatrics Paper on MMR and Autism, CDC Study (2010 ) on Thimerosal and Risk of Autism, Infant and Environmental Exposures to Thimerosal 2007 Study, Narcolepsy Following Pandemrix Influenza Vaccination in Europe, CISA Resources for Healthcare Professionals, Accessing Data from Vaccine Safety Datalink, Frequently Asked Questions and Troubleshooting, U.S. Department of Health & Human Services. Although every vaccine goes through years of testing before being used, vaccines or vaccine lots (specific batches) can also be withdrawn or recalled. Health Canada and the Public Health Agency of Canada have been monitoring this condition since it was raised as a potential safety concern by the European Medicines Agency in April 2021. The InspectIR COVID-19 Breathalyzer test is the first COVID-19 diagnostic test that detects chemical compounds in breath samples associated with SARS-CoV-2 infection. What vaccine is being offered for children ages 5 - 11 years of age. House Committee on Energy & Commerce Hearing: Oversight of the Trump Administrations Response to the COVID-19 Pandemic, FDA Commissioner Stephen M. Hahn, M.D., will be testifying for the FDA.Written testimony, Remarks by Commissioner Stephen Hahn, M.D.The COVID-19 PandemicFinding Solutions, Applying Lessons Learned, Commissioner Hahn speaks to the Alliance for a Stronger FDA, Hearing - COVID-19: Safely Getting Back to Work and Back to School, FDA Commissioner Stephen M. Hahn testified before the U.S. Senate Committee on Health, Education, Labor and Pensions, NIH to launch public-private partnership to speed COVID-19 vaccine and treatment options.

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