2022 - Batch Record Review and Product Release

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. 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).
AREA COVERED
Regulatory requirements for Batch Record Review
What to look for while reviewing batch records, i.e Good Documentation Practices, Compliance to Critical Quality Attributes and Critical Processing Parameters
Skills and Responsibilities of an Effective Batch Record Reviewer
Tools for Effective Batch Record Review
Ensuring Production and Quality Reviewers Coincide with their Reviews
Extensive Training plan for Batch Record Reviewers and when they can be Considered "Qualified" to Review a Record
WHO WILL BENEFIT?
Quality Assurance Batch Record Reviewers
Production Personnel
Production Managers who Review Batch Records
SPEAKER PROFILE
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.
For more detail, please click on this below link:
https://bit.ly/3J7lLbI
Email: info-AT-247compliance.us
Tel: +1-661-336-9555
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