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Validation of Cleaning Processes for Sterile Medical Devices

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A NSF-DBA Medical Devices Course designed and prepared for the Medical Device industry

Dates: Wednesday 23 October 2025
Venue:
AMP Technology Centre, Sheffield, UK
Cost:

£600 excl. VAT

Type: Medical Devices

About this course

This one-day course is intended to provide an introduction to validation of cleaning processes applied during the design and manufacture of sterile medical devices.

This course is designed to provide you with practical advice on what to do to satisfy current regulatory expectations in relation to the validation and routine control of cleaning processes used in the manufacture of sterile medical devices.

What You Will Learn

  • Principles of product cleanliness and definitions of cleanliness
  • How to manage a cleaning validation including what to look for and how to ‘measure’ cleanliness
  • The risks associated with poor cleanliness and the potential consequences to manufacturers
  • About current work on standards associated with cleanliness (including the use of ISO 10993-1 in assessing biological safety)

Who Should Attend

The course is designed for Development Engineers, Manufacturing Engineers, Validation Engineers, Quality Assurance and Regulatory personnel involved in the design, validation and routine control of cleaning processes used during the manufacture of sterile medical devices.

This course forms part of the ‘Managing Cleanrooms & Sterile Medical Device Products’ suite

Enjoy a discount by attending more than one course in this suite. Speak to our team at NSF-DBA for further details

Quick links

NSF-DBA have offices in Kirkbymoorside and Sheffield, UK and Boston and Ann Arbor, USA

A word from NSF-DBA

If you do not find the course you are looking for please contact me at the NSF-DBA Kirkbymooorside Office

Bev Willett, Course Administrator, NSF-DBA

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