London, United Kingdom, March 11, 2016 --(PR.com
)-- The current European medical device directive will be replaced by new regulations that will significantly change and increase the compliance requirements for medical devices and in vitro diagnostic medical devices.
This masterclass aims to address these changes by providing an interactive opportunity to gain a good understanding of the new requirements and thus enable attendees to start planning for future compliance.
This will be achieved as the workshop will feature key sessions on essential requirements, clinical evaluation, conformity assessment, post-market surveillance and end with a brainstorming session.
Carefully selected for his vast array of experience, the workshop will be led by Mika Reinikainen, Managing Director, AbNovo Ltd. Building up over 30 years’ experience within the industry, Mika is currently a member of the European Commission's Medical Device Expert Group and has previously served as European Vice President for of the Regulatory Affairs Professional Society (RAPS) making him the perfect host for this workshop.
To register or for further information on the workshop or workshop leader please visit www.smi-online.co.uk/medicaldevice-api.asp
Compliance with the New Regulations for Medical Devices and In Vitro Diagnostic Products
4th April 2016, Central London, UK
Hosted by: Mika Reinikainen, Managing Director, AbNovo Ltd
Established since 1993, the SMi Group is a global event-production company that specializes in Business-to-Business Conferences, Workshops, Masterclasses and online Communities. We create and deliver events in the Defence, Security, Energy, Utilities, Finance and Pharmaceutical industries. We pride ourselves on having access to the world’s most forward thinking opinion leaders and visionaries, allowing us to bring our communities together to Learn, Engage, Share and Network. More information can be found at http://www.smi-online.co.uk