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Radiation-Emitting Products | FDA

Radiation-emitting products run the gamut from diagnosing serious medical conditions through such things as X-rays and mammograms to helping ensure the safety of airports and office buildings with security X-rays to maki
https://www.fda.gov/radiation-emitting-products - Details - Similar

Search for FDA Guidance Documents | FDA

Search for official FDA guidance documents and other regulatory guidance.
https://www.fda.gov/regulatory-information/search-fda-guidance-documents - Details - Similar

Advisory Committees | FDA

Information about FDA public advisory committees, calendar of meetings, meeting materials, how to become an advisory committee member, guidance, and frequently asked questions.
https://www.fda.gov/advisory-committees - Details - Similar

Where and How to Dispose of Unused Medicines | FDA

The best way to dispose of your expired, unwanted, or unused medicines is through a drug take back program. Or you can do it at home. Check the FDA flush list.
https://www.fda.gov/consumers/consumer-updates/where-and-how-dispose-unused-medicines - 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

The 7 Worst Radiation Dangers In Your Home - Get The Facts!

Are there really dangerous levels of RF (radio frequency) Radiation in my home? The truth in today s world is yes , very much so. Often very dangerous levels of radiation! So if this is true what are the worst radiation
https://www.radiationhealthrisks.com/worst-radiation-dangers-in-home/ - Details - Similar

Who we are

South African Health Product Regulatory Authority is an entity of the National Department of Health, created by the South African Government.
https://www.sahpra.org.za/who-we-are/ - 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

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

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

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