| Greetings!
We are pleased to invite you to Level 2 of the Batch Record Review workshop, where we will dive deeper into the more complex aspects of GMP compliance. This session is designed for professionals looking to enhance their skills in handling variances, deviations, and out-of-specification (OOS) results in batch records. During this workshop, participants will learn advanced techniques to evaluate critical discrepancies, conduct detailed investigations, and apply Corrective and Preventive Actions (CAPA) effectively. Additionally, the workshop will cover best practices for reviewing analytical data and technical documentation, ensuring both product quality and full regulatory compliance.
This workshop is ideal for professionals who already have experience in batch record review or have attended Level 1. It will be particularly beneficial for quality assurance (QA) professionals, regulatory compliance specialists, and anyone involved in in-depth batch record analysis, especially when addressing deviations and OOS investigations.
Throughout the session, you will master advanced techniques in batch record review and gain practical knowledge on investigating variances and handling discrepancies. You will also explore how to review analytical data and technical documentation within batch records, with a focus on ensuring compliance with Good Manufacturing Practices (GMP). The workshop will also guide you on how to implement CAPA in response to batch discrepancies, helping you maintain a continuous improvement cycle and meet regulatory standards.
This session promises to equip you with the tools and strategies necessary to handle complex batch record reviews with confidence. If you're looking to advance your expertise and deepen your understanding of GMP compliance, this workshop is an invaluable opportunity. | 
No comments:
Post a Comment