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Found 7763 results for any of the keywords fda on. Time 0.007 seconds.

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

Contact FDA | FDA

Contact information for the U.S. Food and Drug Administration.
https://www.fda.gov/about-fda/contact-fda - Details - Similar

FDA en español | FDA

La FDA es responsable de proteger la salud pública asegurando la seguridad, eficacia y protección de los medicamentos, los productos biológicos y los dispositivos médicos humanos y veterinarios; y asegurando la seguridad
https://www.fda.gov/fda-en-espanol - 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

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 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

Recalls, Market Withdrawals, Safety Alerts | FDA

FDA and industry press releases regarding product recalls
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts - 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

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