Keep Updated With Clinical Data, Post Market Surveillance and Future Developments Including The Recast
Gain a concise overview of what to expect from The Recast from the EU Commission
For the first time,drivers of the recast, key objectives and timelines are discussed.
Member states collaborate in an exclusive session on clinical evaluation
A dynamic panel discussion will take place whereby speaker-audience interaction is guaranteed
Challenges are discussed and solutions offered from industry specialists
Industry talk about how they have found the last nine months; what has work well and what had proved difficult in regards to the revised directive. Attend this conference to compare industry and to find solutions to the problem areas that are proving to be challanging.
Inquisitive presentations and case studies ensure that your PMS concerns are addressed
Abbotts Vascular, Johnson & Johnson and BSI review the requirements derived from revised Directive 93/42/EC and discuss experiences gained under the new regime.
The literature route verus clinical study
Clarification by Notified Bodies as to when you should use literature and when to conduct a clinical study. A case study is also provided to help you conduct an efficient literature review
Past Events
Medical Device Directive And Future Recast 2011 - 26-27 Jan 2011, Renaissance Brussels Hotel, Belgium (10858)
Important
Please, check "Medical Device Directive And Future Recast" official website for possible changes, before making any traveling arrangements
