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Reprocessing Medical Devices: Approaches and Considerations for Manual Cleaning Validations
This webinar will assist medical device designers and manufacturers navigate the reprocessing requirements and successfully execute a manual cleaning validation. This program will present various aspects of manual cleaning validation testing: overall considerations, selection of artificial test soil, soil challenge sites and dwell time, cleaning reagents, manual cleaning techniques, rinse requirements, and acceptance criteria. It will also cover life cycle considerations and challenges in the design of an appropriate validation study.
If the Reprocessing Medical Devices: Approaches and Considerations for Manual Cleaning Validations is important to your business, act now and make the appropriate connections. See the contact information below.
Relevant job functions include:
Engineering - Biomedical, Design, Manufacturing/Production, Packaging, Process, Project, Quality, R&D
Manufacturing (Packaging, Process)
Research & Development
Regulatory / Compliance / Quality Assurance
Sales / Business Development / Marketing
The session will also benefit pharmaceutical, biotechnology and dental product manufacturers.
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