Efficient and Effective Batch Record Reviews to Improve your Process Capabilities.

Danielle DeLucy

Starting at

$349


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Batch Record Review is a critical part of your operations. This practice is both a vital component to your quality efforts, and a global regulatory requirement. Your firm’s production efforts must be carefully documented. Standard Operating Procedures (SOPs), process controls, and deviations all fall under the purview of batch control. If your efforts are clear, concise, and repeatable, then you have nothing to fear. If your batch control documents are difficult to read, sloppy or worse – non-existent – then look forward to a litany of sanctions, recalls, and costly delays.

 

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. The production and manufacture of pharmaceuticals, biologics, medical devices, etc., involve critical processing parameters. In order to properly document these processing parameters, a strong batch record review system is essential. This webinar with expert speaker Danielle DeLucy, MS, will analyze each of these necessary elements of the batch record review process.

Areas 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 can they be considered “qualified” to review a record

Who will Benefit

  • Quality Assurance batch record reviewers
  • Production personnel and Production Managers who review batch records
  • Compliance Auditors
  • Manufacturing Management & Scientist
Webinar Events
Live -Coming soon!

Training CD-DVD

Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment


Recorded video

Recorded video session



Speaker: 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, 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.


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