21 CFR PART 820 (The Regulations)

Topic	Replies	Views	Activity
About the 21 CFR PART 820 (THE REGS) category	0	1383	February 8, 2016
Software validation - network and computer system validation	3	2071	August 1, 2018
Validation of an ERP System	7	2765	April 25, 2016
New product qualification with ETO sterilisation (Validated Process)	0	1058	May 21, 2014
Training records - signatures	2	1547	September 29, 2013
Vendor qualified software on a database version that isn't qualified by the vendor	1	1144	June 14, 2013
Requirements for QA to sign at the end?	6	1587	May 16, 2013
Automatic validation of data by the system	2	1158	January 11, 2013
PRODUCT REGISTRATION DOSSIER in C.T.D format	3	1400	December 6, 2012
ERP system on a multi-tenant host	2	1346	June 11, 2012
EO and Gamma Product Adoption	0	1412	March 22, 2012
Revalidation for Materials Change	4	1453	March 20, 2012
Paper printouts	4	1600	March 15, 2012
Audit Trails and the Meaning of Independent	0	1148	November 28, 2011
An Easy to Understand Guide - 21 CFR PART 11	0	1125	November 9, 2011
Definition	6	1674	August 25, 2011
What doe the term Biometrics refer to?	4	1576	August 25, 2011
Microbiolgy	2	1379	August 25, 2011
Number of lots	3	2354	August 25, 2011
Holding Time Studies on the Formulated Ready to Fill Bulk	2	1476	June 3, 2011
Weighing balance	9	7589	March 1, 2011
Define: Open Systems	4	1834	August 18, 2010
ERP validation	2	1372	June 10, 2010
FDA warning letters	1	1268	December 24, 2008
Products made during validation	1	1149	November 21, 2008
Electronic records in lieu of paper records	3	1399	September 29, 2008
Informatique files and two site of production	2	1212	August 8, 2008
Simple part 11 compliance for one system	9	1917	July 22, 2008
Validation of a software Implementation	5	1406	June 24, 2008
Hplc	1	1164	May 6, 2008