Key Questions on Compliance with New Regulations for Medical Devices and In Vitro Diagnostic Products Addressed This April
SMi Training's CPD accredited masterclass: “Compliance with the New Regulations for Medical Devices and In Vitro Diagnostic Products” will take place on the 4th April in London, UK.
London, United Kingdom, February 19, 2016 --(PR.com)-- This masterclass will allow attendees to plan for full compliance ahead of the new medical device regulations which are expected to be implemented just before April 2016. The timing of this event creates the perfect opportunity for attendees as it will allow a fresh insight into upcoming regulatory updates.
The workshop will address the following:
• What are the fundamental changes?
• What impact this will have for attendees?
• What are the technical standards and essential requirements for risk assessment?
• Post mark surveillance plan: What are the key requirements for effective clinical follow ups; vigilance and management of adverse reactions?
Carefully selected for his experience, with over 30 years in the medical device field; the workshop will be led by Mika Reinikainen Managing Director of AbNova Ltd. Mika set up his own medical device consulting company, Abnovo Ltd, which focuses on regulatory strategy and compliance as well as manufacturers’ conflicts with Notified Bodies and Competent Authorities. He was directly involved in the development of the Medical Devices Directives and of technical standards and is currently a member of the European Commission’s Medical Device Expert Group and of the Commission’s Working Groups on Borderlines and Classification as well as New & Emerging Technologies.
With his vast array of experiences, Mika poses as the perfect host for ‘Compliance with the New Regulations for Medical Devices and In Vitro Diagnostic Products 2016’ and will ensure attendees get the most out of this workshop.
For those who are interested in attending this interactive workshop, there is currently a £50 discount available online which expires on 29th February.
Further information including a PDF brochure is available online at: 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
www.smi-online.co.uk/medicaldevice-api.asp
About SMi:
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
The workshop will address the following:
• What are the fundamental changes?
• What impact this will have for attendees?
• What are the technical standards and essential requirements for risk assessment?
• Post mark surveillance plan: What are the key requirements for effective clinical follow ups; vigilance and management of adverse reactions?
Carefully selected for his experience, with over 30 years in the medical device field; the workshop will be led by Mika Reinikainen Managing Director of AbNova Ltd. Mika set up his own medical device consulting company, Abnovo Ltd, which focuses on regulatory strategy and compliance as well as manufacturers’ conflicts with Notified Bodies and Competent Authorities. He was directly involved in the development of the Medical Devices Directives and of technical standards and is currently a member of the European Commission’s Medical Device Expert Group and of the Commission’s Working Groups on Borderlines and Classification as well as New & Emerging Technologies.
With his vast array of experiences, Mika poses as the perfect host for ‘Compliance with the New Regulations for Medical Devices and In Vitro Diagnostic Products 2016’ and will ensure attendees get the most out of this workshop.
For those who are interested in attending this interactive workshop, there is currently a £50 discount available online which expires on 29th February.
Further information including a PDF brochure is available online at: 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
www.smi-online.co.uk/medicaldevice-api.asp
About SMi:
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
Contact
SMi Group
Teri Arri
+44 20 7827 6162
http://www.smi-online.co.uk/medicaldevice-api.asp
Teri Arri
+44 20 7827 6162
http://www.smi-online.co.uk/medicaldevice-api.asp
Contact
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