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4 Hour Virtual Seminar on Batch Record Review and Product Release

5126
Duration : 6 Hours

Danielle DeLucy, Pharmaceuticals, Biotechnology

Danielle DeLucy, MS, is owner of ASA Training and Consulting, LLC which provides Pharmaceutical and Biologics based companies with training and quality systems assistance in order to meet Regulatory compliance. Prior to this role, Danielle has been in the industry for 15 years serving in numerous Quality Management Roles, suc Read more


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.

Course Objectives:

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)

Course Outline:

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

Methods for Batch Record Review

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

Methods for Data Review and Actions taken for Deviations

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

Case Study - Review of a Mock Batch Production Record

What You Get:

• Training Materials
• Live Q&A Session with our Expert
• Participation Certificate
• Access to Signup Community (Optional)
• Reward Points

Who Will Benefit:

• Quality Assurance batch record reviewers
• Production personnel and Production Managers who review batch records
• Compliance Auditors
• Manufacturing Management & Scientist
• Other professionals who review batch records

Please reach us at 1-888-844-8963 for any further assistance or if you wish to register

100% MONEY BACK GUARANTEED

Refund / Cancellation policy

Get In Touch

Subject : 4 Hour Virtual Seminar on Batch Record Review and Product Release


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