Following the success of CTMD2015, held in Vienna, Austria, CTMD2016 will continue to focus on the latest developments and upcoming regulations on clinical trials for medical devices internationally. Deciding on a clinical site and investigator? Lost in the regulatory maze?
CTMD2016 is a pragmatic event directed at filtering through the information overload of the digital age to deliver targeted information. CTMD2016 will directly address the hot topics in the field of medical device clinical trials:
Selecting a clinical site and investigator
Understanding the process for obtaining approval to conduct a clinical trial
What are the new regulations for planning and executing clinical trials?
Participants at CTMD2016 will once again have the unique opportunity to gain first-hand knowledge from key opinion leaders by scheduling one-on-one meetings during the coffee and lunch breaks at the congress. CTMD2016 would like to welcome professionals worldwide with a target audience of CEOs, general managers, R&D personnel, clinical professionals, regulatory affairs specialists, engineers, CROs, application specialists and QA personnel.
We look forward to seeing you at CTMD2016 in the exciting and historical city of Berlin.
|Contact No. :||+44 203 051 4032|
|Registration Type||End Date||Price|
|Full Participant Registration||15 Sep,2016||USD 950.00|
|Full Participant - On-Site Registration||21 Sep,2016||USD 1100.00|