Press release content from Business Wire. The AP news staff was not involved in its creation.
PRESS RELEASE: Paid content from Business Wire
Press release content from Business Wire. The AP news staff was not involved in its creation.

6-Hour Virtual Seminar on Batch Record Review & Product Release, 2019 - ResearchAndMarkets.com

May 16, 2019 GMT

DUBLIN--(BUSINESS WIRE)--May 16, 2019--

The “6-Hour Virtual Seminar on Batch Record Review and Product Release” webinar has been added to ResearchAndMarkets.com’s offering.

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 Should You 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)


I. Regulatory Requirements for GMP Documents - Batch Records & Beyond

  • Review Good documentation requirements for batch records
  • Types of Regulated documents and relative importance
    • Master Batch Record Templates - Control and Issuance
    • Manufacturing Records - In process and final product
    • Specifications - Quality Review
    • Investigations - Deviation and Out of Specifications
    • Change Control Process

II. Methods for Batch Record Review

  • Defining the Review process
  • Batch Record SOP development
  • Roles and responsibilities of reviewers both Quality and Operations
  • Effective review practices and tools to identify discrepancies

III. Methods for Data Review and Actions taken for Deviations

  • Review of Analytical Data
  • Out-of Specification test results and deviations

IV. Case Study - Review of a Mock Batch Production Record

For more information about this webinar visit https://www.researchandmarkets.com/r/4rb095

View source version on businesswire.com:https://www.businesswire.com/news/home/20190516005886/en/

CONTACT: ResearchAndMarkets.com

Laura Wood, Senior Press Manager


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Related Topics:Medical Devices,Pharmaceutical Manufacturing



SOURCE: Research and Markets

Copyright Business Wire 2019.


PUB: 05/16/2019 12:16 PM/DISC: 05/16/2019 12:16 PM