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Online Webinar 2019 - 4-Hour Virtual Seminar - Batch Record Review and Product Release

Date2019-08-20

Deadline2019-08-20

VenueOnine, USA - United States USA - United States

Keywords

Websitehttps://www.eventbrite.com/e/4-hour-virt...4456477058

Topics/Call fo Papers

Session Highlights
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
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
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.
Speaker
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 17 years serving in numerous Quality Management Roles, such as the Director of Product Quality, the oversight of Sterility Assurance practices and provided QA oversight of numerous filling and packaging operations. Danielle began her QA career as a Quality Control Pharmaceutical Microbiologist at a contract laboratory where she performed various tests for their clients. In the years after, she has held positions in the Quality management arena while increasing her responsibility. She has helped to lead many Regulatory Health Inspections and was instrumental in the coaching process of her peers prior to any inspection. Currently, Danielle assists companies who are faced with warning letters, consent decrees and those wishing to improve compliance establish more robust quality systems so that the company can succeed.

Last modified: 2019-08-12 19:55:39