Description

Training Outcomes

Understanding best cleanroom practice.
Preparing for and keeping up to date with forthcoming changes in standards and regulations.
Identify realistic cost and energy saving opportunities.

Focus A concentrated course providing the attendee an opportunity to get and keep right up to date with essential standards and best practice for cleanrooms intended for life sciences applications.

Review of current cleanroom classification requirements and use of BS/EN/ISO 14644-1 and 2.
A heads up on the revision of ISO 14644-1 & 2. The new statistical model.
Best practice for air filtration.
Cleanroom monitoring.
Integration with The GMPs for sterile products. Impact on industry.
Sustainable design and operation of cleanrooms and clean air devices.

Who Should Attend?

Cleanroom users in manufacturing and research.
Specifiers, consultants, and project managers.
Suppliers and installation firms
QA and QC professionals
Certification and test houses.
Validation personnel.

Trainer Gordon Farquharson, a Chartered Engineer with more than 30 years experience in quality and safety engineering systems used by the pharmaceutical and life sciences industry. He is a cleanroom expert, is convenor of ISO TC 209, and has been active in the revision of the EU, PIC/S, and WHO GMPs for sterile products.