RQM+

Founded in 2020 from the merger between R&Q and Maetrics, but with roots going back to the 1980s, RQM+ is the largest medical device and diagnostics focused full-service regulatory and quality consulting firm in the world. It is privately owned, with offices in the US, the UK, and Switzerland.

Global Headquarters
RQM+
2790 Mosside Blvd
Suite 800
Monroeville
PA 15146
United States

Phone / Contact

T: +1 877 652 0830

Articles by RQM+

Dr Celeste Maksim

MDR COMPLIANCE: PLANNING FOR POST-MARKET CLINICAL FOLLOW-UP

Celeste Maksim discusses best practices for drug delivery device manufacturers when conducting post-market clinical follow-up activities, as mandated by the EU Medical Device Regulation.

ECONOMIC OPERATORS UNDER THE EU MDR: THE NEW REQUIREMENTS

Beth Crandall spells out the new requirements for Economic Operators under the EU Medical Device Regulation.

EU MDR DEADLINE DELAY: WHAT DOES IT MEAN FOR THE MEDICAL DEVICE INDUSTRY?

With the compliance deadline for the EU Medical Device Regulation recently delayed by a year due to the novel coronavirus pandemic, Beth Crandall looks at what it means for the medical device industry.

EU MDR: ANCILLARY DELIVERY DEVICES FACE EQUAL SCRUTINY TO STANDALONE MEDICAL DEVICES

Elizma Parry offers her expertise and practical guidance to businesses hoping to achieve a CE mark for a medical device, with new EU regulations being implemented this year.

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