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2014 - Introduction to ISO 13485: Medical devices?Quality management systems?Requirements for regulatory purposes
Topics/Call fo Papers
Medical Device
Other CFPs
- Understanding, Reporting and Documenting HIPAA Breaches
- Fundamentals of Medical Device Design Controls
- Regulatory Strategies for Marketing and Selling a Mobile Medical Device and Medical Applications (Apps) for Use on Smartphones and Similar Mobile Devices
- How to Develop a Master Validation Plan
- FDA 510(k) Update: Trends, New Strategy, Submission and FDA Clearance
Last modified: 2014-02-19 13:36:55