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About the REGULATORY TRENDS AND QA category
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0
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1165
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February 8, 2016
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Eu fmd
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2
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1372
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May 25, 2019
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PDA Technical Report 3, Revised 2013
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2
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3617
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January 14, 2019
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QA Review of QA documents
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1
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1300
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August 22, 2018
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Product Quality Review
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0
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1405
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July 4, 2018
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Stability extrapolation
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6
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5382
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March 28, 2018
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Use of API in his last month of validity
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4
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1367
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February 1, 2018
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Plastic containers in Pharma industry during production process?
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1
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1299
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October 13, 2017
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Effectiveness Evaluation
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1
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1279
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September 18, 2017
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How to report the Description as per USP
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1
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1841
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August 21, 2017
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[New Course] 21 CFR Part 820 Subpart C
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0
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1329
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September 28, 2016
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The Similarity Between Device Master Records & Chocolate Chip Cookies [Video]
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0
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1395
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September 28, 2016
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Training Path - QA
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6
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2150
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July 28, 2016
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Change Control Follow Up-When To close it?
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5
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2705
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May 19, 2016
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New EU GMP Annex 16 - Certification by a Qualified Person and Batch Release
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1
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1939
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December 1, 2015
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WHO GUIDANCE ON GOOD DATA AND RECORD MANAGEMENT PRACTICES - draft for comment
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0
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2226
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November 5, 2015
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Chinese GMP Annex on Computer systems
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0
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1589
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August 12, 2015
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New on toxicological evaluation
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0
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1583
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July 1, 2015
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New EU GMP Annex 15 - Qualification and Validation published
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1
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1658
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April 7, 2015
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Specification: Acceptance criteria
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0
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1166
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January 11, 2015
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EMA published final Guideline on Setting health base exposure limits (PDE)
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0
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1381
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November 27, 2014
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New validation
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2
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1387
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October 30, 2014
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Draft ISO/DIS14644-1.2, ISO/DIS14644-2.2 and ISO/DIS14644-14 recently published
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0
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1721
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October 19, 2014
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Revised PIC/S GMP Guide
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1
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1498
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August 25, 2014
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DCP & CEP Queries
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1
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1639
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May 21, 2014
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EMEA Draft : Process validation for Biotech derived products
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0
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1317
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May 14, 2014
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FDA Draft :Clinical Pharmacology Data-Bio similars
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0
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1157
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May 14, 2014
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FDA Guidance: Allowable Excess Volume in Injectables
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0
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1236
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March 18, 2014
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PDMA Update: Preapproval GMP guidance
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0
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1395
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February 25, 2014
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FDA Draft: Analytical Procedures and Methods Validation
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0
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1370
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February 21, 2014
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