Cleaning Validation Course

In the pharmaceutical industry, the cleanliness of production equipment is not just a matter of good practice but a regulatory mandate. Contaminants like dust, microbes, and residual substances can compromise the safety and efficacy of pharmaceutical products. The “Cleaning Validation” course is designed to provide a comprehensive understanding of how to perform and validate cleaning to meet stringent GMP regulations effectively.

Who should be enrolled ? This vital training is designed for Quality Assurance and Quality Control specialists, production managers, and operational staff within the pharmaceutical sector.

Guided by Dr. Jefferson, a seasoned CAPA Manager with extensive industry experience, attendees will gain practical skills to prevent contamination risks. Dr. Jefferson’s background ensures the course material is grounded in real-world applications, providing participants with strategies to maintain product integrity and regulatory compliance.

Completing the course awards a unique, shareable, and verifiable certificate, signifying a mastery of the principles and practices necessary to manage and certify clean manufacturing environments.

Curriculum:

Lesson 1: Introduction

Lesson 2: Scope of Cleaning Validation

Lesson 3: General Guidelines

Lesson 4: Cleaning Validation Process

Lesson 5: Acceptance Criteria

Conclusion

Evaluation