About the 21 CFR PART 820 (THE REGS) category
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0
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1462
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February 8, 2016
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Software validation - network and computer system validation
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3
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2187
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August 1, 2018
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Validation of an ERP System
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7
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2901
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April 25, 2016
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New product qualification with ETO sterilisation (Validated Process)
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0
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1145
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May 21, 2014
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Training records - signatures
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2
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1690
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September 29, 2013
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Vendor qualified software on a database version that isn't qualified by the vendor
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1
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1224
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June 14, 2013
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Requirements for QA to sign at the end?
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6
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1705
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May 16, 2013
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Automatic validation of data by the system
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2
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1227
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January 11, 2013
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PRODUCT REGISTRATION DOSSIER in C.T.D format
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3
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1545
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December 6, 2012
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ERP system on a multi-tenant host
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2
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1466
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June 11, 2012
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EO and Gamma Product Adoption
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0
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1543
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March 22, 2012
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Revalidation for Materials Change
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4
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1567
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March 20, 2012
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Paper printouts
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4
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1728
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March 15, 2012
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Audit Trails and the Meaning of Independent
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0
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1256
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November 28, 2011
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An Easy to Understand Guide - 21 CFR PART 11
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0
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1225
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November 9, 2011
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Definition
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6
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1796
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August 25, 2011
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What doe the term Biometrics refer to?
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4
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1690
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August 25, 2011
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Microbiolgy
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2
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1492
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August 25, 2011
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Number of lots
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3
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2504
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August 25, 2011
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Holding Time Studies on the Formulated Ready to Fill Bulk
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2
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1567
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June 3, 2011
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Weighing balance
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9
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7758
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March 1, 2011
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Define: Open Systems
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4
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1943
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August 18, 2010
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ERP validation
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2
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1499
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June 10, 2010
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FDA warning letters
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1
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1352
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December 24, 2008
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Products made during validation
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1
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1281
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November 21, 2008
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Electronic records in lieu of paper records
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3
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1518
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September 29, 2008
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Informatique files and two site of production
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2
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1326
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August 8, 2008
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Simple part 11 compliance for one system
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9
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2057
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July 22, 2008
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Validation of a software Implementation
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5
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1486
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June 24, 2008
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Hplc
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1
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1266
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May 6, 2008
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