MedTech I.Q.

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

Event Details

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

Time: July 8, 2019 from 8am to 2pm
Location: Online
Street: 39658 Mission Boulevard, Fremont, CA 94539, USA
City/Town: Fremont
Website or Map: http://www.globalcompliancepa…
Phone: 8004479407
Event Type: virtual, seminar
Organized By: John Robinson
Latest Activity: Jul 3

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Event Description

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.

Why you should attend

  • Recognize regulatory requirements for batch records and batch record review
  • Discover the essentials of batch record reviewer qualifications and training
  • Establish a working relationship between production and quality reviewers
  • What to do when a batch fails to meet specifications (discrepancies and deviations)

Who Will Benefit

  • Quality Assurance batch record reviewers
  • Production personnel and Production Managers who review batch records

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