About the Course

This Aseptic Processing training course is suitable for all members of staff working with aseptic processes in sterile product manufacturing operations, introduce new thinking to your site and team for process validation and risk assessment.

It is well understood that sterility of an aseptic product cannot be determined by direct assessment of the finished product. Therefore, microbiological safety of the product can only be achieved by careful assessment of the hazards and control measures in place to provide the confidence that the items are safe for the patient and fit for use.

Historically aseptic processes have relied heavily on monitoring of the environment, air, surfaces and personnel to verify the success of the process. However, modern aseptic processes require a more holistic assessment of all the protective measures in place within the process and the complex interaction between these control measures, this approach is fully covered within this course.

We guarantee that on completion of this course, with the knowledge gained, you will look at aseptic processing from a new perspective.

To view our full range of training courses please download the Honeyman Training Prospectus.  Book your place now or enquire about our other Pharma Courses – Honeyman Training

For practical assistance with outsourced monitoring for contamination control in pharmaceutical manufacturing visit www.honeymanlaboratories.com

Who Should Attend This Aseptic Processing Training Course?

• QP’s and Quality
• Operational Managers
• Operations Personnel
• Operational Managers
• Operational Managers

Aseptic Processing Training Course Objectives

• To understand the fundamental mechanisms of contamination transfer from source to product and the protective measures in place to prevent product contamination.
• To have the opportunity to work with risk management techniques like HACCP and RMC through practical workshops.
• To understand the technology associated with cleanrooms and aseptic processes and understand the key control measures and they impact the sterility assurance of the product.
• To introduce new thinking for validation and risk assessment of the process.
• To understand the cGMP regulations and guidelines for aseptic processing and to engage in discussions regarding industry changes and best practice.