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Process Validation Guidance Requirements (FDA and EU Annex 15: Qualifications and Validation)

 
  March 09, 2022  
     
 
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).
 
 
Organized by: ComplianceOnline
Invited Speakers: Barry A. Friedman,

 
Deadline for Abstracts: March 31 - April 1, 2022
 
Registration:
$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


E-mail: referral@complianceonline.com
 
   
 
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