Introduction to this course: 

This course will focus on physical contaminants after a general description of different types of contaminants. It will cover contamination sources, cleanroom protocols, and best practices in manufacturing environments. Gain essential skills to protect patient safety and maintain compliance with industry regulations in the life sciences. 

Who should attend: 

This course is ideal for pharmaceutical professionals, including quality control and assurance specialists, production managers, GMP auditors, and regulatory affairs personnel. It's also beneficial for cleanroom operators, microbiologists, and chemical analysts involved in drug manufacturing. 

Learning Outcomes: 

By the end of this lesson, you will be able to:

• Describe the types and sources of physical, chemical, and microbial contaminants in pharmaceutical environments.

• Implement cleanroom protocols and best practices to minimize contamination risks.

• Identify potential contamination points in manufacturing processes and develop mitigation strategies.

What will I gain: 

Participants will gain a comprehensive understanding of contamination control, enabling them to ensure the safety and efficacy of pharmaceutical products and medical devices. They will acquire practical skills to implement and evaluate contamination control measures in compliance with industry standards.

Prerequisites: 

Prerequisites for this course include basic knowledge of pharmaceutical manufacturing processes and familiarity with industry regulations.

Additional information: 

Course duration: 00:21:27

Course code/version (effective date): L-104/v1.0 (10/05/2023)