An Introduction to the Medical Devices Directive 2015 provides a detailed introduction to the European medical device legislation.
An Introduction to the Medical Devices Directive 2015 covers topics such as:
- Know what a Competent Authority expects
- Learn the role of a Notified Body
- Comply with Manufacturing Responsibilities
- Better under Conformity Assessment Procedures, Classification, Medical Device legislation
- Plan your Clinical Evaltuions
- Consider the requirements for Quality Systems
An Introduction to the Medical Devices Directive 2015 brings together:
- Pharmacovigilance
- Regulatory Affairs
- Technical Support
- Quality Assurance