2021 - 6-Hour Virtual Seminar on Batch Record Review and Product Release
Date2021-01-21
Deadline2021-01-19
VenueFremont, USA - United States
KeywordsQuality Assurance; Production Managers; Virtual Seminar
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.
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.
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Last modified: 2020-12-15 18:50:44