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About the WHITE PAPERS category
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0
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1185
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February 8, 2016
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Stability chambers
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3
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1520
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May 8, 2018
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A Validation Approach for LIMS
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2
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1314
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March 12, 2014
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Writing Effective Test Scripts
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2
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1342
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April 3, 2013
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How to achieve international action on falsified and substandard medicines
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0
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1174
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November 20, 2012
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50 Acronyms of the FDA
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0
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1128
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November 11, 2012
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Alternative SWD Models to the V-Model
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0
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1197
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June 14, 2012
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Process validation latest guideline from USFDA
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1
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1335
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March 21, 2012
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Usfda guidelines
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6
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1835
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March 10, 2012
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Annex 11 Vs CFR's
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2
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1268
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August 25, 2011
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Latest guideline on SMF from PIC's
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1
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1322
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July 25, 2011
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Suppliar qualification latest guidelines from APIC
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0
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1243
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May 31, 2011
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Quality by Design for ANDA
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5
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1708
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April 8, 2011
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Link between sunlight and drug efficacy
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0
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1208
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March 16, 2011
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CMO consolidation
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0
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1155
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March 15, 2011
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Prequalification programme for selected APIs
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0
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1021
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March 12, 2011
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$1.3bn average R&D cost per new drug
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0
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1154
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March 12, 2011
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Cancer trials biggest risk for Pharmas
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0
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1327
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February 19, 2011
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Fda mapp
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0
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1235
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February 18, 2011
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Huge step Forward by EU
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0
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1228
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February 18, 2011
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Method Validation
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0
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1459
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February 10, 2011
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Residual solvents
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0
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1352
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February 7, 2011
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Forced Degredation Studies
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0
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1160
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February 7, 2011
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GxP assessment form
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4
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2419
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January 3, 2011
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Retooling for Traceability: 10 Steps
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0
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1130
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December 25, 2010
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Monographs Pharmacopoeias in Scribd
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0
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1700
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December 16, 2010
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Impurities in Pharmaceuticals
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2
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1338
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December 9, 2010
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Changes in European pharmacopoeia - Microbiology
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0
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1253
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December 9, 2010
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FDA launches global supply chain pilot scheme-News
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0
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1170
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December 3, 2010
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Guidelines needed for inconsistent OTC medication -News
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0
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1178
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December 3, 2010
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