NAMSA’s MRO Summits bring thought leadership and industry professionals directly to you! These complimentary, intimate gatherings allow for expert discussions and shared experiences in medical device development. Within a few hours’ time, you will hear presentations, panel conversations and experiential learning, and will be a part of a day devoted to the art of efficient medical device development. Ultimately, you will leave the summit with recommendations, updates, guidance and resources critical to your device development process, as well as tools to help you on the path to becoming the expert.

Please join us at these complimentary events, coming to a city near you. Please refer to the list of locations below and associated registration links within the location name (where available) to learn more.

January 18, 2017 – Columbus, OH
Topics Include: Preclinical; Global Regulations; Clinical Research

February 22, 2017  – Minneapolis, MN
Topics Include: Preclinical; Global Regulations; Clinical Research

March 7, 2017  – Arlington Heights, IL
Topics Include: Leveraging Material & Testing Data; Global Regulations; Clinical Research

March 28, 2017 – Campbell, CA
Topics Include: Validation, Sterilization & Reprocessing of Medical Devices; Global Regulations; Clinical Research

April 2017 – Copenhagen, Denmark (Info coming soon!)
Topics Include:  Leveraging Material and Testing Data; Global Regulations; Clinical Research

April 6, 2017 – Stuttgart Germany
Topics Include: Leveraging Material & Testing Data; Global Regulations; Clinical Research

April 25, 2017 – Waltham, MA
Topics Include: Leveraging Material & Testing Data; Global Regulations; Clinical Research

April 27, 2017 – Edison, NJ
Topics Include: Leveraging Material & Testing Data; Global Regulations; Clinical Research

May 9, 2017 – Raleigh, NC
Topics Include: Preclinical; Global Regulations; Clinical Research

May 11, 2017 – Atlanta, GA
Topics Include:  Preclinical; Global Regulations; Clinical Research

June 13, 2017 – Manchester, UK 
Topics Include: Leveraging Material & Testing Data; Global Regulations; Clinical Research

June 15, 2017 – Lyon, France
Topics Include: Validation, Sterilization & Reprocessing of Medical Devices; Leveraging Material & Testing Data; New MDR regulatory impact

Summer 2017 – Houston, TX (Info coming soon!)
Topics Include: Leveraging Material & Testing Data; Global Regulations; Clinical Research

Fall 2017 – Salt Lake City, UT (Info coming soon!)
Topics Include: Leveraging Material & Testing Data; Global Regulations; Clinical Research