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2021 - 6-Hour Virtual Seminar on Batch Record Review and Product Release

Date2021-01-21

Deadline2021-01-19

VenueFremont, USA - United States USA - United States

KeywordsPharmaceuticals; Virtual Seminar; Quality Management

Websitehttps://www.planurevents.com/virtual-sem...

Topics/Call fo Papers

Overview
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.

Last modified: 2020-12-15 18:25:42