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2020 - Reviewing Drug Product Batch Records
Date2020-07-09
Deadline2020-06-29
VenueOnline event, USA - United States 
KeywordsPharmaceutical production; Quality by design; Batch record review
Topics/Call fo Papers
Regulatory requirements for batch review (EU and US)
Important areas to check in batch records
Common errors
Examples of deficiencies leading to regulatory enforcement action
Overview of the draft ICH Q12 guidance
ICH Q12 and Quality by Design
Benefits of continuous improvement
Approaches to data trending
Important areas to check in batch records
Common errors
Examples of deficiencies leading to regulatory enforcement action
Overview of the draft ICH Q12 guidance
ICH Q12 and Quality by Design
Benefits of continuous improvement
Approaches to data trending
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Last modified: 2020-05-19 19:31:49