About the Course
Introduction to this course:
Dive into best practices for minimizing contamination in drug, vaccine, and biological production. Explore critical areas such as sterilization methods, environmental controls, single-use technologies, and the latest aseptic processing techniques. Learn to adhere to strict regulatory standards and ensure product safety and efficacy.
Who should attend:
This course is intended for manufacturing professionals, quality assurance and quality control personnel, regulatory affairs personnel, microbiologists, production managers, and anyone involved in pharmaceutical manufacturing, biologics production, and quality assurance.
Learning Outcomes:
By the end of this lesson, you will be able to:
Recall key principles of aseptic processing, including contamination sources and sterilization techniques.
Implement effective aseptic techniques and environmental controls in pharmaceutical and biological production settings.
What will I gain:
Participants will gain in-depth knowledge of aseptic processing, sterilization methods, and contamination control strategies.
Prerequisites:
Prerequisites for this course include a basic understanding of fundamental concepts in drug production and quality control.
Additional information:
Course duration: 00:09:42
Course code/version (effective date): L-1011/v1.0 (28/02/2024)
Course Categories
-
How to minimize contamination in aseptic processing
- Lesson 1: Key strategies to minimize contamination
- Lesson 2: Environmental monitoring and single-use technologies
- Milestone_Videos_Lesson 1 to Lesson 2
-
Additional resources
- Mind map: Sterilie Medicinal Products
-
Survey
- Course survey
About the Course
Introduction to this course:
Dive into best practices for minimizing contamination in drug, vaccine, and biological production. Explore critical areas such as sterilization methods, environmental controls, single-use technologies, and the latest aseptic processing techniques. Learn to adhere to strict regulatory standards and ensure product safety and efficacy.
Who should attend:
This course is intended for manufacturing professionals, quality assurance and quality control personnel, regulatory affairs personnel, microbiologists, production managers, and anyone involved in pharmaceutical manufacturing, biologics production, and quality assurance.
Learning Outcomes:
By the end of this lesson, you will be able to:
Recall key principles of aseptic processing, including contamination sources and sterilization techniques.
Implement effective aseptic techniques and environmental controls in pharmaceutical and biological production settings.
What will I gain:
Participants will gain in-depth knowledge of aseptic processing, sterilization methods, and contamination control strategies.
Prerequisites:
Prerequisites for this course include a basic understanding of fundamental concepts in drug production and quality control.
Additional information:
Course duration: 00:09:42
Course code/version (effective date): L-1011/v1.0 (28/02/2024)
-
How to minimize contamination in aseptic processing
- Lesson 1: Key strategies to minimize contamination
- Lesson 2: Environmental monitoring and single-use technologies
- Milestone_Videos_Lesson 1 to Lesson 2
-
Additional resources
- Mind map: Sterilie Medicinal Products
-
Survey
- Course survey