New Hyde Park, New York – Cleanliness is a hot topic in the medical device industry. The FDA expects medical device companies to validate the cleanliness of their devices. One of the best ways to achieve a clean device is by designing it with cleanliness in mind.
Why attend
This Compliance Globoal webinar will provide valuable guidance to medical device manufacturers on design considerations for both single-use and re-usable devices. There are certain design elements that are more difficult to clean and should be avoided whenever possible. With the right design, both the manufacturing and cleaning process validation can be simplified.
Areas covered
- Design requirements document
- Single-use design considerations
- Re-usable design considerations
- Design elements to avoid/minimize
- Simplifying the manufacturing process
- Simplifying the cleaning process
Objectives
- Why cleaning must be considered during the design phase
- What design elements should be avoided or minimized
- What can be done to simplify the manufacturing and cleaning processes
- Who benefits
- QA/QC Managers and Personnel
- Validation Managers and Personnel
- R&D Professionals
- Engineering Professionals
- Compliance Officer
- Marketing & Sales
Level
- Beginner
Source: Compliance Global