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