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45 mins

Computer System Validation (CSV) – Basic Concepts, Regulations and GAMP®5

11/29/2017

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Microbiological Contamination of Pharmaceutical Products – Part 1

10/24/2017

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21 CFR Part 820 Subpart H – Acceptance Activities

08/31/2017

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21 CFR Part 820 Subpart G – Production and Process Controls

06/08/2017

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How To Be An Effective GMP Auditor – Part 3

06/05/2017

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How to be an Effective GMP Auditor – Part 1

05/10/2017

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21 CFR Part 820 Subpart E – Purchasing Controls

01/26/2017

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21 CFR Part 11 – Electronic Signatures

10/25/2016

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21 CFR Part 11 – Electronic Records

10/12/2016

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21 CFR Part 820 Subpart D – Document Controls

09/28/2016

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