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.
|Conference/Event Dates:||10/26/2016 - 10/26/2016|
|Other Industries:||Manufacturing, Medical|
|Audience:||Senior level executives involved in regulatory affairs for medical device companies, including those from manufacturing services providers, consulting companies, product development, and financial/investment companies and government.
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.
|Booth Size||Booth Cost||Available Amenities|
|Marketing Vehicles Allowed:||n/a|
|Other Booth Sizes Available: n/a|
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