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MedWatch: The FDA Safety Information and Adverse Event Reporting Progr

MedWatch is made up of voluntary and mandatory reporting on prescription medicines, over-the-counter medicines, non-vaccine biologicals, medical devices, special nutritional products, cosmetics and non-prescription human
https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program - Details - Similar

COVID-19, Flu and RSV | FDA

COVID, Flu and RSV vaccines, tests, and treatments - information about FDA-approved and authorized medical products for seasonal respiratory illnesses
https://www.fda.gov/consumers/covid-19-flu-and-rsv - Details - Similar

Public meeting: FDA Rare Disease Day 2024 - 03/01/2024 | FDA

FDA will host Rare Disease Day, a virtual public meeting, on March 1, 2024 in global observance of Rare Disease Week. This year's Rare Disease Day is dedicated to patients and health care professionals.
https://www.fda.gov/news-events/fda-meetings-conferences-and-workshops/public-meeting-fda-rare-disease-day-2024-03012024 - Details - Similar

FDA Voices | FDA

Insights from FDA leadership and experts into the agency s work on policy, consumer safety enforcement, medical products, food, tobacco.
https://www.fda.gov/news-events/fda-newsroom/fda-voices - Details - Similar

U.S. Food and Drug Administration

The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation s f
https://www.fda.gov/ - Details - Similar

FDA revises letter of authorization for the emergency use authorizatio

FDA revises letter of authorization for the emergency use authorization for Paxlovid
https://www.fda.gov/drugs/drug-safety-and-availability/fda-revises-letter-authorization-emergency-use-authorization-paxlovid - Details - Similar

Microwave Ovens | FDA

Microwave oven manufacturers are required to certify their products and meet safety performance standards created and enforced by the FDA to protect the public health.
https://www.fda.gov/radiation-emitting-products/resources-you-radiation-emitting-products/microwave-ovens - Details - Similar

Electronic Common Technical Document (eCTD) | FDA

Electronic Common Technical Document (eCTD) mandatory use for some submissions starts May 2017. eCTD is the standard format for electronic reg submissions.
https://www.fda.gov/drugs/electronic-regulatory-submission-and-review/electronic-common-technical-document-ectd - Details - Similar

Expiration Dating Extension | FDA

In some cases, testing has shown that certain properly stored medical products can be used beyond their labeled expiration date if they retain their stability. Recognizing MCM stockpiling challenges, FDA is engaged, when
https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/expiration-dating-extension - Details - Similar

Drug Shortages | FDA

The .gov means it’s official.Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
https://www.fda.gov/drugs/drug-safety-and-availability/drug-shortages - Details - Similar

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