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Aseptic Manufacturing of Pharmaceutical Products

The course covers one of the most challenging and high risk activities undertaken by the pharmaceutical and bio-pharmaceutical industry. To operate effectively in the field of aseptic manufacturing, it is essential to understand the sources/basic mechanisms of contamination in conjunction with the associated systems and procedures required to effectively control such contamination. This course provides attendees with an in-depth appreciation of contamination sources and mechanisms, together with effective controlling and monitoring mechanisms such as: good cleanroom operation; effective facility/HVAC system design, operation and maintenance; good aseptic behaviours/disciplines; effective personnel clothing systems, sterilisation processes, Aseptic Process Simulation (APS), risk management initiatives and environmental monitoring. All the latest regulatory requirements are built into the course's presentations.

Delegates will be provided with a 3-slide per page printed binder upon arrival on Day 1 and PDF versions of the slides will be sent out by email to each delegate after the course. Day-time meals and refreshments, together with a course dinner, held on the evening of Day 1 (Tuesday 3 Sep 2024), are included in the overall package.


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September 2024
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Tuesday, 3rd September 2024 to Thursday, 5th September 2024 (3 days)

Hotel Scandic Copenhagen, Denmark, Copenhagen, Denmark

09:00 - 17:00

£2,500 per delegate

NOTE: Course fees will be subject to a 20% UK VAT charge if your billing/invoice address is in the UK and/or delegates are UK based