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ComplianceOnline, online event
March 31 - April 1, 2022
The Process Validation Guidelines (January 2011) and the EU Annex 15: Qualification and Validation (October 2015) outline the general principles and approaches the two regulatory bodies consider appropriate elements of process validation for the manufacture of human and animal drugs and biological products, including Active Pharmaceutical Ingredients (APIs).
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Organized by:
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ComplianceOnline |
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Invited Speakers:
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Barry A. Friedman,
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Deadline for Abstracts:
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March 31 - April 1, 2022
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Registration:
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$1,299* (Seminar for One Registration) Mar 31 - April 1, 2022, Virtual Seminar Register now and save $600 (ActualPrice: $1,899) https://www.complianceonline.com/fda-eu-annex15-ich-process-validation-qualification-cgmp-ppq-seminar-training-80375SEM-prdsm?channel=hum-molgen
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E-mail:
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referral@complianceonline.com
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