2016, September 21-22
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 3 ‘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.