This one day course is designed to support manufacturers by confirming current regulatory requirements of technical documentation. The aim of the course is to help you better manage the Notified Body certification process and enable manufacturers to sell compliant devices within the European Union.
On completion of training you will be able to identify and locate all regulatory requirements and guidance documentation necessary to write procedures enabling the creation and maintenance of compliant technical files and design dossiers.
How will I benefit?
- Generate technical documentation that support safe products that perform as intended meeting regulatory requirements – first time
- Place products on the market in line with your critical launch dates
- Reduce costs by streamlining the certification process
Who should attend?
- Regulatory, Design and Development Professionals
- Quality Managers
- Clinical Affairs Specialists
- Production Managers
What will I learn?
On completion of this training, participants will be able to:
- Confirm the technical documentation requirements as specified in the Directive
- Interpret the general requirements of the Directive using relevant and harmonized standards together with various European & GHTF guidance documents for specific products
- Define the process enabling the creation and maintenance of compliant technical files and design dossiers
- Explain the Notified Body certification process and level of response required to questions and nonconformities raised
What's included?
- You will gain 8 CPD points on completing the course
- Training course notes
- Lunch
- Refreshments
Course Guide
