2020 - 6-Hour Virtual Seminar - Batch Record Review and Product Release
Date2020-09-03
Deadline2020-09-08
VenueOnline, USA - United States
KeywordsQuality Assurance; Production Managers; Pharmaceuticals
Topics/Call fo Papers
Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate compliance.
A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc.
This webinar will analyze each of these necessary elements of the batch record review process.
A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc.
This webinar will analyze each of these necessary elements of the batch record review process.
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Last modified: 2020-08-17 16:39:40