Are you ready to implement the new Medical Device regulations, particularly focusing on PMS and economic operators?
The Medical Device Regulations are due for significant updates with areas such as Post Market Surveillance and Economic Operators being major areas of change. The final form of the regulations is now set and due to be voted into European Law. The new regulations need to be considered now at all organisational levels as they will be impacting decisions taken today.
MedilinkWM, in conjunction with Acclaim Biomedical Consulting, is offering a one day workshop exploring the new European Regulations for Medical Devices. With over 20 years experience in Medical Devices, Acclaim Biomedical Consulting are best placed to support and advise on the regulatory changes and the impact these will have on existing practice.
The course is aimed to provide attendees with the insight and tools to plan and implement their organisations strategy for continued access to the European market by the deadlines set in the new regulations. The course is designed to review critical elements of the new regulations and will be run as an interactive 1 day course designed for business leaders with a good working knowledge of current requirements.
Course Content and Key Topics Covered
- Review of critical elements of the new regulations
- Understanding the ares of change
- Assess the business impacts
- How to develop strategic solutions to ensure compliance
Who should attend
- Medical Device Manufacturers
- Regulatory Affairs Officers and Managers
- Quality Control Officers and Managers
Medilink Member: £140 + VAT
Non-member: £190 + VAT
To find out more information or register your place, please click here.