About the WHITE PAPERS category
|
|
0
|
935
|
February 8, 2016
|
Stability chambers
|
|
3
|
1279
|
May 8, 2018
|
A Validation Approach for LIMS
|
|
2
|
1115
|
March 12, 2014
|
Writing Effective Test Scripts
|
|
2
|
1079
|
April 3, 2013
|
How to achieve international action on falsified and substandard medicines
|
|
0
|
1032
|
November 20, 2012
|
50 Acronyms of the FDA
|
|
0
|
912
|
November 11, 2012
|
Alternative SWD Models to the V-Model
|
|
0
|
974
|
June 14, 2012
|
Process validation latest guideline from USFDA
|
|
1
|
1095
|
March 21, 2012
|
Usfda guidelines
|
|
6
|
1583
|
March 10, 2012
|
Annex 11 Vs CFR's
|
|
2
|
1079
|
August 25, 2011
|
Latest guideline on SMF from PIC's
|
|
1
|
1084
|
July 25, 2011
|
Suppliar qualification latest guidelines from APIC
|
|
0
|
1051
|
May 31, 2011
|
Quality by Design for ANDA
|
|
5
|
1460
|
April 8, 2011
|
Link between sunlight and drug efficacy
|
|
0
|
944
|
March 16, 2011
|
CMO consolidation
|
|
0
|
957
|
March 15, 2011
|
Prequalification programme for selected APIs
|
|
0
|
804
|
March 12, 2011
|
$1.3bn average R&D cost per new drug
|
|
0
|
978
|
March 12, 2011
|
Cancer trials biggest risk for Pharmas
|
|
0
|
1052
|
February 19, 2011
|
Fda mapp
|
|
0
|
995
|
February 18, 2011
|
Huge step Forward by EU
|
|
0
|
1043
|
February 18, 2011
|
Method Validation
|
|
0
|
1162
|
February 10, 2011
|
Residual solvents
|
|
0
|
1092
|
February 7, 2011
|
Forced Degredation Studies
|
|
0
|
971
|
February 7, 2011
|
GxP assessment form
|
|
4
|
2216
|
January 3, 2011
|
Retooling for Traceability: 10 Steps
|
|
0
|
904
|
December 25, 2010
|
Monographs Pharmacopoeias in Scribd
|
|
0
|
1477
|
December 16, 2010
|
Impurities in Pharmaceuticals
|
|
2
|
1070
|
December 9, 2010
|
Changes in European pharmacopoeia - Microbiology
|
|
0
|
1024
|
December 9, 2010
|
FDA launches global supply chain pilot scheme-News
|
|
0
|
962
|
December 3, 2010
|
Guidelines needed for inconsistent OTC medication -News
|
|
0
|
956
|
December 3, 2010
|