10times
28 Jan 2021Ended

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

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Estimated Turnout

upto 100
Delegates
Based on previous editions

Editions

Jan 2021
+2 more editions

Frequency

Quarterly
Next edition likely in Apr 2021
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Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch .. Read more records. Recorded: Access recorded version, only for one participant unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar). Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar). 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.

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