MedilinkWM, 4 Greenfield Crescent, Edgbaston, B15 3BE
The final text of the new regulations has now been published, now is the time to gain a detailed understanding of the European compliance landscape which is going to dictate business strategy for the next 20 years.
MedilinkWM, in conjunction with Acclaim Biomedical Consulting, is offering a one day workshop exploring the new European Regulations for In Vitro Diagnostics. 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.
Course Content and Key Topics
Risk Based Product Classification
Obligations of Economic Operators
This course aims to provide delegates with the insight and tools required to plan and implement an organisational strategy for continued access to the European Markets. The course will review critical elements of the new regulations in great depth and will run as a full day, interactive course.
From this workshop you will take away our specially made checklist, that will assist you with making sure that your organisation is working in line with the new Regulations
Who should attend?
The course is designed for business leaders with a good working knowledge of the current regulatory requirements
Early bird fee: Register before Friday 14th April to take advantage of the 10% discount
Members Fee: £150
Non Member Fee: £190
Lunch and refreshments provided
For more information regarding the course and booking, please contact Vanessa Bailey
Telephone: 0121 452 5630