An Introduction to the Design and Development of Medical Devices
This intensive two-day course will introduce those who are new to medical device design and development to the critical elements of the process. It has been designed to provide delegates with an insight into the tools and techniques required to design and develop a medical device and offer an essential overview of the current regulatory landscape. The importance of safety and efficacy will be covered, as will risk management and documentation. As combination products are a huge market, the programme will also address device constituent parts of combination products.
Attending this event will provide delegates with a comprehensive appraisal of key aspects of this process and an opportunity to discuss the complexities involved with an experienced industry expert.
Benefits of attending:- Gain a comprehensive overview of the design and development process
- Comply with the regulatory requirements and standards
- Learn about design controls
- Review materials and biocompatibility
- Access key information on documentation management and systems
- Understand how risk should be managed
- Consider human factors and usability studies
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Reviews by course attendees
Average rating 4.3
Good pace. Mixture of text and graphics... David did a good job and was engaging considering that the course was online, which is always difficult.
Mr. Howlett was very forthcoming, open to questions, and he really poured his expertise in the training, which made all the difference... I liked a lot the first day about desig...
I would recommend it to anyone with no experience of design controlled medical device development. A good overview with a good amount of detail.