MEDICAL DEVICE 21 CFR PART 820 (The Regulations)
| Topic | Replies | Views | Activity | |
|---|---|---|---|---|
|
What are they thinking?
|
|
4 | 1086 | January 22, 2008 |
|
Intended of FEA (CADCAM) software
|
|
3 | 1088 | August 29, 2007 |
|
FDA Clinical Requirements
|
|
0 | 789 | June 18, 2007 |
|
GAMP 5: What to expect!
|
|
3 | 1264 | June 6, 2007 |
|
Questions & Answer's from Audit Trail FDANews Audioconference
|
|
0 | 628 | May 25, 2007 |
|
FDAnews.com - Audioconference in May/June
|
|
0 | 739 | March 23, 2007 |
|
Electronic Signatures Explained
|
|
5 | 1481 | March 14, 2007 |
|
Environmental Monitoring issue
|
|
1 | 1110 | March 9, 2007 |
|
Regulatory requirement for deleting a User Id record from a GxP
|
|
0 | 1263 | January 22, 2007 |
|
Part 11 testing how much is required
|
|
1 | 915 | January 16, 2007 |
|
21 CFR Part 211.68 Summary
|
|
0 | 1301 | November 6, 2006 |
|
What are the controls for a closed system
|
|
0 | 650 | October 23, 2006 |
|
Define: Electronic Signatures
|
|
0 | 793 | October 23, 2006 |
|
What is the definition of an electronic record
|
|
0 | 993 | October 23, 2006 |
|
What is a closed system?
|
|
0 | 1338 | October 23, 2006 |