PRISYM ID to Exhibit and Speak at the American Medical Device Summit
PRISYM ID will be exhibiting and Tim Fischer will be speaking at the American Medical Device Summit in Chicago, IL on the 4/5th October 2017, stand 24.
Setting the standard on how the industry should connect and exchange ideas, the Generis American Medical Device Summit provides insights and strategies to enhance the professional development of executives involved in the design, development and manufacturing of medical devices.
The event is held over two days, with thought provoking content and exceptional networking potential. Over 200 industry peers can explore the challenges and opportunities in medical device development, quality management, speed to commercialization, and regulatory harmonization.
PRISYM ID is a Thought Leadership Partner for the event and it will be delivering a presentation within a workshop session, entitled “Be ready for the EU MDR Labeling and use the lessons learnt from UDI” to address these regulatory procedures and will highlight the benefits of its flagship, label life-cycle management solution, PRISYM 360.
Changing regulations, such as evolving UDI, EU MDR or the EU clinical trial regulations, need to be incorporated into the label and artwork medical device manufacturing processes appropriately, and in time for when the regulation takes effect.
The presentation will be held on 5 October from 12:35 pm to 1:10 pm and Tim Fischer will be the speaker.
For more information about PRISYM ID or to arrange a meeting during the event, please contact firstname.lastname@example.org or call +44 (0)118 936 4400
Read our blog: Survey reveals that only 17% of the respondents are aware of the changes that come with the EU MDR