Management of Cleanrooms for the Manufacturing of Sterile Pharmaceutical Products

£1070 + VAT

2nd - 3rd July 2008

This new course provides an extensive introduction to the regulatory requirements governing pharmaceutical cleanroom operation and details the methods for producing sterile products and the issues surrounding both aseptic and terminal sterilisation manufacture. 

From this course delegates will develop an appreciation of the significance of sterile products to the patient and understand why there is intensive regulatory interest in the control of sterile (in particular aseptic) manufacture. 

Course Content:

• The importance of sterility
• Basic microbiology
• Terminal sterilisation and aseptic manufacture
• GMP requirements for controlled environments
• Facility design, classification and operation
• Facility validation
• Environmental monitoring
• Media fills
• People issues

To book a training course, please download the booking form, complete and email to bookings@rssl.com