MEDICAL DEVICE

Topic	Replies	Views	Activity
ERP system on a multi-tenant host 21 CFR PART 820 (The Regulations)	2	1509	June 11, 2012
EO and Gamma Product Adoption 21 CFR PART 820 (The Regulations)	0	1590	March 22, 2012
Revalidation for Materials Change 21 CFR PART 820 (The Regulations)	4	1616	March 20, 2012
Paper printouts 21 CFR PART 820 (The Regulations)	4	1787	March 15, 2012
Audit Trails and the Meaning of Independent 21 CFR PART 820 (The Regulations)	0	1298	November 28, 2011
An Easy to Understand Guide - 21 CFR PART 11 21 CFR PART 820 (The Regulations)	0	1270	November 9, 2011
Definition 21 CFR PART 820 (The Regulations)	6	1849	August 25, 2011
What doe the term Biometrics refer to? 21 CFR PART 820 (The Regulations)	4	1742	August 25, 2011
Microbiolgy 21 CFR PART 820 (The Regulations)	2	1544	August 25, 2011
Number of lots 21 CFR PART 820 (The Regulations)	3	2611	August 25, 2011
Holding Time Studies on the Formulated Ready to Fill Bulk 21 CFR PART 820 (The Regulations)	2	1624	June 3, 2011
Weighing balance 21 CFR PART 820 (The Regulations)	9	7829	March 1, 2011
Define: Open Systems 21 CFR PART 820 (The Regulations)	4	1994	August 18, 2010
ERP validation 21 CFR PART 820 (The Regulations)	2	1543	June 10, 2010
FDA warning letters 21 CFR PART 820 (The Regulations)	1	1401	December 24, 2008
Products made during validation 21 CFR PART 820 (The Regulations)	1	1356	November 21, 2008
Electronic records in lieu of paper records 21 CFR PART 820 (The Regulations)	3	1568	September 29, 2008
Informatique files and two site of production 21 CFR PART 820 (The Regulations)	2	1375	August 8, 2008
Simple part 11 compliance for one system 21 CFR PART 820 (The Regulations)	9	2125	July 22, 2008
Validation of a software Implementation 21 CFR PART 820 (The Regulations)	5	1514	June 24, 2008
Hplc 21 CFR PART 820 (The Regulations)	1	1299	May 6, 2008
What are they thinking? 21 CFR PART 820 (The Regulations)	4	1118	January 22, 2008
Intended of FEA (CADCAM) software 21 CFR PART 820 (The Regulations)	3	1116	August 29, 2007
FDA Clinical Requirements 21 CFR PART 820 (The Regulations)	0	816	June 18, 2007
GAMP 5: What to expect! 21 CFR PART 820 (The Regulations)	3	1298	June 6, 2007
Questions & Answer's from Audit Trail FDANews Audioconference 21 CFR PART 820 (The Regulations)	0	654	May 25, 2007
FDAnews.com - Audioconference in May/June 21 CFR PART 820 (The Regulations)	0	768	March 23, 2007
Electronic Signatures Explained 21 CFR PART 820 (The Regulations)	5	1566	March 14, 2007
Environmental Monitoring issue 21 CFR PART 820 (The Regulations)	1	1142	March 9, 2007
Regulatory requirement for deleting a User Id record from a GxP 21 CFR PART 820 (The Regulations)	0	1323	January 22, 2007