Webinars Archive

Showing 17–32 of 34 results

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  Sterile Filtration in Biopharmaceutical Manufacturing: Technical Overview, Trends and Regulatory

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  Re-scheduled Control of Cleanroom Garments and Supplies: Contamination Control

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  EU GMP Annex 1 and Pharmig’s response (pre-recorded)

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  Microbial control of pharmaceutical water systems

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  Which identification system is right for you?

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  Control of Cleanroom Garments and Supplies: Contamination Control

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  EU GMP Annex 1 and Pharmig’s response

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  Operation of Sterility Testing Isolators and Validation Issues

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  Depyrogenation & Depyrogenation Studies

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  Fungal Contamination in Pharmaceutical Products and Cleanroom Risk

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  Best Practice in the Effective Management of Sterility Test Failures

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  ISO 14644 Updates – Free to 2016 Pharmig Members

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  Data Integrity and New Expectations – Thursday 17th September 2pm – 3pm (GMT)

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  Disinfection/Sanitisation Processes: cGMP for Cleaning and Disinfection

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  GMP Chapters & Interpretation of – 3,5,6 & 8

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  Microbiological Risk of Personnel and Cleanrooms

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