Course Content:
- Introduction & Course Objectives
- An overview of the medical device sector in Ireland / Globally
- What are medical devices and how do they work
- Regulations that govern the medical device sector – ISO 13485:2016 and 21 CFR Part 820 and 93/42 EEC
- How Medical devices are classified and brought to Market within Europe, USA and Canada
- The role of Regulatory Bodies : Competent Authority – Health Products Regulatory Authority, FDA and notified bodies BSI,NSAI TUV etc – role within manufacturing
- The role of Cleanrooms and classification of cleanrooms
- Good Documentation Practice (GDP)
- Work Instructions
- Change Control
- Good Manufacturing Practice.
- Device Design Systems
- Basic Problem Solving Techniques
- Q&A
- Conclude & Follow Up Process