Successful completion provides learners with a dated, traceable and downloadable certificate for the course :
Each certificate is CPD/CEU accredited and 21 CFR PART 11 compliant. Certificates validity can be checked online through our certificate online checker. They can also be shared on Linkedin.
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.
Lesson 1: Introduction
Lesson 2: Scope of Cleaning Validation
Lesson 3: General Guidelines
Lesson 4: Cleaning Validation Process
Lesson 5: Acceptance Criteria