Research and Markets Offers Report An Introduction to Post Marketing Surveillance and the European Medical Device Vigilance (Course, London) [Professional Services Close - Up]
(Professional Services Close - Up Via Acquire Media NewsEdge) Research and Markets has announced the addition of the "An Introduction to Post Marketing Surveillance and the European Medical Device Vigilance (Course, London)" conference to its offerings.
In a release, Research and Markets noted that report highlights include:
The An Introduction to Post Marketing Surveillance and the European Medical Device Vigilance Course will be held on 11th December 2013 at The Rembrandt Hotel, London
Gain a Valuable Understanding of this Important Area
A manufacturer's responsibility for a medical device does not come to an end when the device is CE marked and sold on the market. The period after the sale is just as important as the pre-market approval stage. It is during this period that more can be learnt about a device and where the obligations lie with manufacturers to have an appropriate post market surveillance system in place.
This one day practical workshop will introduce you to the concept of post market surveillance, what it is, how to implement it effectively and how to understand and interpret the regulatory requirements for your products. Managing customer complaints successfully will also be addressed. There will be ample time for case study exercises and group discussions throughout the day.
PROGRAMME TO INCLUDE:
- What is Post Market Surveillance (PMS)?
- Discover why PMS is necessary
- The regulations and guidelines; what are they and how should we apply them?
- Understand the purpose of a vigilance system
- Learn how to monitor, manage and report incidents
- Customer complaint handling
- Post Market Clinical Studies (PMCF); how should these be conducted and how should events be reported?
WHO SHOULD ATTEND:
This meeting is appropriate for all those concerned with monitoring and managing the safety and performance aspects of medical devices during the post market phase. This is an introductory course and will therefore be particularly useful for personnel new to a regulatory role which involves post market surveillance, it will also be useful to clinical staff who have a desire to understand more about the vigilance procedures particularly in relation to management, monitoring and reporting of adverse incidents.
It will also be applicable to support staff and those wishing to gain a better understanding of the post market surveillance and vigilance procedures in general, where it may be necessary to have some knowledge to be able to carry out their duties.
Delegates will receive a course material folder containing comprehensive documentation provided by the speakers, which will be a valuable source of reference for the future
A Certificate of Attendance for Professional Development will be given to each participant who completes the course
11 December 2013
Registration & Coffee:
11 December 2013 09.00
Venue and Accommodation:
The Rembrandt Hotel, 11 Thurloe Place,
London SW7 2RS
Opposite V&A Museum. Nearest Underground station: South Kensington.
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