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Title, Username & Date Rating  Last Post  Replies 
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Category
What's the FDA expectation on following Mfg SOPs? Just train & go, or always have the SOP open & fol...
05-04-2009 04:05pm by: Rick wassmuth
9.0
Excellent
Jul 17, 2013
by: Michelle Sceppa
5 2 All FDA Regulated Industry
If the conductivity is 1.31 microSiemens per cm at 25C is it out of specs already; USP says 1.3 micr...
02-18-2009 10:02am by: Josefina susbilla
9.0
Excellent
Jun 04, 2009
by: Venkat
4 2 All FDA Regulated Industry
In process validation, how important is VMP?
09-06-2007 07:09pm by: Rajasekar Rajasekar
9.0
Excellent
Oct 22, 2007
by: Sukhwinder Singh
4 1 All FDA Regulated Industry
How can we qualify old equipments without any documents,though the same are working fine?
05-21-2007 09:05pm by: Sn ghosh
7.0
Good
Jul 17, 2013
by: Dr. ludwig Huber
4 1 All FDA Regulated Industry
what is root cause analysis
04-28-2009 01:04am by: Ravi

Nov 20, 2010
by: Chetan kumar
3 1 FAA Compliance
how capa helps pharmaceutical industry, regards sunil wakhloo
06-05-2007 08:06pm by: Sunil Wakhloo

Oct 21, 2007
by: Jose Mora
3 1 Quality Management
Auditing Systems for 21 CFR Part 11 - Validation
08-27-2013 10:08pm by: Co attendee

Dec 15, 2014
by: Coexpert
2 1 All FDA Regulated Industry
Auditing Systems for 21 CFR Part 11- Validation and Qualification
08-27-2013 09:08pm by: Co attendee

Dec 15, 2014
by: Coexpert
2 1 All FDA Regulated Industry
Time taken to put a security plan together
05-14-2013 02:05am by: Co attendee

Jun 29, 2013
by: Coexpert
2 1 IT Controls and Compliance
Difference between retest date and expiration date for drug substances
02-09-2012 09:02pm by: Co attendee
9.0
Excellent
Feb 21, 2013
by: Coexpert
2 1 Drugs and Chemicals (Pharma)
Differentiate between Deviation Management and CAPA. How CAPA is important to Deviation Management (...
10-24-2007 04:10am by: Prashanth Bbau
9.0
Excellent
Oct 28, 2007
by: Sanjeev Koul
2 1 Quality Management
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