Peter Rose to speak on new MDR at RAPS Regulatory Convergence 2017
Peter Rose, Managing Director for Maetrics operations in Europe, will be speaking at the upcoming RAPS Regulatory Convergence about the new Medical Device Regulation (MDR) in Europe at the National Harbour at the DC Waterfront on Monday 11th September from 3:00PM to 3:45 PM.
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The most important word of the MDSAP acronym is “Single,” because the program is offering an “all-in-one” audit to accommodate multiple legislations. The industry would be well-advised to treat this as a positive change as the collaboration and support amongst the stakeholders will be the most effective and efficient way to implement the Medical […]July 26, 2017
Agreement has finally been reached over the new European Union Medical Device Regulation (MDR) and is expected to come into effect in June 2017. MDR was approved by the European Parliament on April 5, 2017 and was published in the Official Journal of the European Union on 5th May 2017. This new Regulation, whose […]May 24, 2017
Navigating Post Market Surveillance Requirements in International Waters and in a Changing Regulatory
In the EU, specifically, it is crucial for manufacturers to review their systems, processes, and procedures for post market surveillance to ensure that they are compliant not only with the increasingly demanding requirements expected in the new Medical Device Regulation, but also with those of the single countries they distribute to. This must-read guide outlines […]June 22, 2016
UK (September 04, 2017) – Maetrics, a global leader in life science consulting, has appointed Brian Moan to Director of Solutions Delivery in Europe. A highly qualified industry expert and thought leader specializing in Human Factors, Brian has been involved in MHRA working groups to develop industry guidance, has frequently presented around regulatory issues and has developed […]September 19, 2017
Peter Rose, Managing Director for Maetrics operations in Europe, will be speaking at the upcoming RAPS Regulatory Convergence about the new Medical Device Regulation (MDR) in Europe at the National Harbour at the DC Waterfront on Monday 11th September from 3:00PM to 3:45 PM.August 30, 2017
Indianapolis (6/15/17) Maetrics, a global management consulting firm providing life science companies with deep quality, compliance, regulatory solutions to the life sciences industry, recently named Chris Busse as Vice President, Business Development. In this role, Chris will be responsible for further developing our presence in the Western United States and managing key client relationships.June 15, 2017
MEDICA is the world’s largest event for the medical sector. For more than 40 years it has been firmly established on every expert’s calendar. There are many reasons why MEDICA is so unique. Firstly, the event is the largest medical trade fair in the world – in 2016 it attracted more than 5,100 exhibitors from 70 countries […]October 3, 2017
Join us as we learn about the newest changes at the FDA since January 1, 2017; hear a panel discuss the challenges and special efforts that are being made in the world of Cyber Security, and listen to some of the newest adventures into Regenerative Medicine being made that will affect many of our companies […]October 3, 2017
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. Join the discussion with over 200 of your industry peers as we explore the challenges and […]September 15, 2017