This Medilink Professional Development (MPD) event has been developed with Advena Medical Ltd to guide you through the CE marking process. This will offer you a tool box to ensure your organisation’s documentation is up-to-date ahead of the impending new regulations and help to prepare you for the minefield surrounding the Medical Device Directive.

By Attending This Course You Will

Gain an understanding of the mandatory legal requirements for medical devices placed on the market anywhere within the EU.

What’s in it for your Business?

– Increase your company return on investment for research and product development
– Up-skill your workforce

Course Content and Key Topics Covered

– Outline of EU Directives and impeding changes
– EU regulatory structure
– Intended use and device classification
– Standards
– The technical file
– Risk and Quality Management
– Essential Requirements
– Introducing new products, new designs and design validation

Who Should Attend

This course would be relevant for those within the following roles:
– Legal and IP Managers
– Quality/Risk Managers
– Commercial Manager / Director
– Business Development Manager
– Business Consultant
– Design

Delegate Fee

Early Bird Fee: Receive a 10% discount when you book before Friday 31st July2015

Member Fee: £250+VAT
Non-Member Fee: £350+VAT *Eligible SMEs will receive a 50% discount on the listed delegate fee.

To register or for more information please contact Sarah Wootton – 0121 452 5630

This project has been partly supported by HM Government with Employer Ownership funding.

50% of the delegate fee can be reclaimed by MedilinkWM through the SIP Programme meaning the cost to your company is just £125+VAT/ £175+VAT.

Eligibility – Under the Science Industry Partnership (SIP) scheme, eligible companies must be located in England and have less than 250 employees in the UK.