US FOOD AND DRUG ADMINISTRATION (FDA)

Topic	Replies	Views	Activity
About the US FOOD AND DRUG ADMINISTRATION (FDA) category	0	979	February 8, 2016
UDI - tests required for the labels and codes	1	1505	February 9, 2016
FDA approves non-surgical temporary balloon device to treat obesity	0	1083	August 12, 2015
Drug Shortage2 App for Android devices from FDA released	0	1181	August 12, 2015
Welcome to our new forum	2	1353	May 13, 2015
FDA - Possibility of visiting a Supplier?	2	1460	January 30, 2015
FDA GMP requirement: Avoid Non contact with floor? 21 CFR Part 110	1	1270	December 11, 2014
What do we need to do to be certified as a GLP lab?	1	1299	December 11, 2014
Pharma Industry stance on ISO 17025 Accreditation - In-House Calibration Laboratories	1	1191	December 11, 2014
Bench Testing as part of 510(k) Submission	1	1230	December 11, 2014
SW (Software) changes during a pending 510(k)	1	1077	December 11, 2014
Original Data Copying to Maintain Compliance with 21 CFR Part 820.180	1	1169	December 11, 2014
What is the regulation number for Biohazard Bag?	1	1314	December 11, 2014
FDA Medical Device Accessory Packaging Requirements	1	1275	December 11, 2014
List Distributor or Manufacturer	1	1244	December 11, 2014
Three Questions on Finished Medical Device Traceability, Labeling and Packaging	1	1276	December 3, 2014
Electronic Submissions to the FDA	1	1198	December 1, 2014
Titanium Implants MR (Magnetic Resonance) Compatibility Labeling	1	1176	December 1, 2014
Should a contract manufacturer for components be filing MDR exemption?	1	1465	December 1, 2014
New model for existing Class I Device Listing (510K exempt)	1	1238	December 1, 2014
Does FDA expect suppliers to be independently assessed to 21 CFR Part 820?	2	1226	November 12, 2014
Submitting data with Special 510(k)	0	1133	November 6, 2014
How to Notify the FDA When Ownership Changes?	0	1316	November 6, 2014
Class I Device Listing (510K exempt)	0	1077	November 6, 2014