Who Will Benefit:
This 3 hour webinar will provide invaluable assistance to all personnel in the Medical Device industry, who have a stake in expanding their business into a MDSAP participating country and for those interested in more information about MDSAP and how it may apply to them.
This webinar will be particularly useful for those involved in research and development, document creation for regulatory submission, data handling and for those conducting/monitoring/coordinating clinical investigation, performing risk management and post-market vigilance/surveillance. This seminar is a must for those who are looking to apply for a medical device registration and product license in a MDSAP country.
Those employees working in the following roles will significantly benefit by attending:
- Regulatory Affairs
- Quality assurance, quality control, and quality systems
- Product development personnel
- Contract research organizations
- Business management
- Site managers
- Senior and executive management
- Contractors and subcontractors
- Distributors
- Consultants