Clinical Study Approval in the UK

Description:
The environment for conducting medical device studies in the UK has seen many changes in recent years. There are numerous initiatives to encourage device research in the UK and, as a result of this, we are slowly starting to see more device studies being conducted in the UK. The regulators, the research ethics committees, and the institutions where studies are being conducted have all been working towards a quicker, more robust approval process. It is important for anyone considering conducting studies in the UK to understand these new processes and procedures. This eConference will demystify the processes and provide you with the tools you need to conduct successful device studies in the UK.

 

Why should I take this eConference:
Would you like to have the most up to date information on conducting device studies in the UK direct from a UK expert?  Would you like to understand the processes and procedures for gaining fast efficient approvals for conducting studies in the UK?  Would you like to know how much studies cost in the UK, would you like to know about the new Device Clinical Trial Agreement, the UKCRN, the changes to the Research Ethics committees.  If your answer is yes to any of these questions then you should attend this eConference.

 

You will learn:
About; The UK environment for conducting device studies.

 

You will get:
-Slides of the presentation.
-Advice, instructions documentation and information on conducting device studies sin the UK.
-Chance to hear other's q&A.
-0.15 CEU.

 

This eConference is designed for anyone currently conducting device studies in the UK or considering doing so.

 

Presenter

Clinical Device Group is proud to present Mrs. Janette Benaddi RGN, BSc, MICR, MIOD Janette Benaddi is the CEO of Medvance™ Ltd.  Medvance provides consultancy in medical device clinical research and regulatory affairs. Janette has 18 years experience in managing medical device studies.  Prior to founding Medvance almost 10 years ago Janette worked for several medical device manufacturers in marketing, regulatory and clinical roles. Janette is a registered nurse has a BSc and Diploma in Management Studies, a Diploma in Company Direction and holds a teaching certificate.  She is a Board Director of the Institute of Clinical Research and is also currently Chairman of the Institutes Medical Device Committee.  Janette has published a number of articles related to medical devices and sits on several committees involved in the regulation and standardization of medical device studies.  For many years Janette has been working closely with the UK regulators Research Ethics Committees and other bodies based in the UK in order to improve UK processes and make the UK a more attractive country in which to conduct device studies.  She has been instrumental in pushing forward a number of progressive initiatives within the UK. You can reach Ms. Benaddi at Janette@medvance.co.uk

 

The purchase is $403 for the CD. Event materials are available on the CD itself. Each attendee is eligible for 0.15 CEUs upon completing the course feedback via the link provided with the event materials. Click here to purchase.