Manufacturing Sterile Products

14 December 2016, Reading, United Kingdom


Introduction
Course Scope:
This course provides an extensive introduction to the regulatory requirements governing pharmaceutical clean room operation, and details the aseptic filling and terminal sterilisation methods for producing sterile products. The delegates will gain an appreciation of the significance of sterile products to the patient, and understand why there is intensive regulatory interest worldwide in the control of sterile product manufacture.

Overview:
At the end of the course you will:
•Understand the risks associated with sterile products
•Appreciate the requirements for contamination control and how this links to clean room design
•Understand the methods for terminal sterilisation and processes involved in aseptic product manufacture
•Appreciate the importance of people and the need for trained personnel

Who should attend:

This course will provide valuable underpinning knowledge to all personnel working for companies responsible for the manufacture of sterile products. It will be of benefit to those working in sterile products manufacturing, QC (especially environmental monitoring personnel), QA personnel as well as support engineers.
Venue
RSSL Training

Training room, RSSL Training, The Science and Technology Centre, Earley Gate, Whiteknights Road, Reading, RG6 6BZ, United Kingdom

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Contact information
Customer Services
RSSL
+44(0)118 918 4076
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