| Greetings!
We’re pleased to announce the upcoming Batch Record Review Level 1 workshop, designed to help professionals build a strong foundation in Good Manufacturing Practices. This session introduces the principles that define effective documentation, production controls, and compliance in regulated environments. Participants will explore the structure and purpose of batch records, understand regulatory expectations, and learn how accurate record-keeping directly supports product quality and patient safety.
The workshop provides a practical introduction to reviewing batch records, identifying discrepancies, and understanding the flow of GMP documentation. It also offers guidance on how to manage minor variances, interpret deviations, and ensure that documentation meets compliance standards.
Whether you are new to regulatory affairs, quality assurance, or manufacturing, this program helps you develop the habits and attention to detail that form the backbone of quality systems.
Through a combination of structured instruction and discussion, you will gain clarity on the standards that govern the pharmaceutical and biotechnology industries, building the confidence to apply those principles in your daily work. | 
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