Press Releases

Dec — 2017

MCRA Offers Informational Presentation on Medical Device Regulation to the Chinese FDA

NEW YORK, Dec.

Nov — 2017

MCRA Leads Innovation Training with FDA as Part of its Experiential Learning Program (ELP)

The Experiential Learning Program (ELP) is a learning opportunity designed to help all levels of FDA within the Center for Devices and Radiological

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Sep — 2017

FDA Selects MCRA to Share Expertise as Part of the Experiential Learning Program (ELP)

The Experiential Learning Program (ELP) is a program designed to help all levels of FDA within the Center for Devices and Radiological Health (CDRH

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Jul — 2017

MCRA Releases New White Paper Analyzing the Industry Impact of the Federal Budget Request on FDA

As the medical device market grows due to continued innovation and changing demographics, it is imperative for industry to be able to successfully

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Jul — 2017

MCRA Advises Orthopedic Industry To Adopt Integrated Value Creation Strategy

Mr.

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Feb — 2017

MCRA Expands, Moves to New DC Location

WASHINGTON, Feb.

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Aug — 2016

SANUWAVE Health Submits de novo Petition for FDA Review and Classification of the dermaPACE System to Treat Diabetic Foot Ulcers

ALPHARETTA, Ga., Aug. 11, 2016 (GLOBE NEWSWIRE) -- SANUWAVE Health, Inc. (OTCBB:SNWV) today announced that it has submitted to the U.S.

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Jul — 2016

MCRA Assists Cartiva, Inc. with Obtaining FDA PMA Approval for the Company's Synthetic Cartilage Implant (SCI)

WASHINGTON, July 20, 2016 /PRNewswire-USNewswire/ -- Musculoskeletal Clinical Regulatory Advisers, LLC (MCRA) announced today its role in

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Jun — 2016

MCRA Assists VertiFlex, Inc. with Obtaining FDA PMA Approval for the Superion® Interspinous Spacer System

WASHINGTON, June 24, 2015 /PRNewswire-USNewswire/ -- Musculoskeletal Clinical Regulatory Advisers, LLC (MCRA) announced today its role in the succe

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Mar — 2016

MCRA Hires Experienced Trauma And Total Joint Expert To Expand Its Leading Orthopedic Regulatory Team

WASHINGTON, March 1, 2016 /PRNewswire-USNewswire/ -- Musculoskeletal Clinical Regulatory Advisers, LLC (MCRA), a leading medical device consul

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Nov — 2014

MCRA Assists Wright Medical Group, Inc. with Obtaining FDA PMA Approvable Decision for Augment® Bone Graft

WASHINGTON, Nov.

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Expand Your Healthcare Distribution With MCRA Global Access

A unique integrated perspective for creating the optimal product pathway

Deep Therapy Experience

Expand Your Healthcare Distribution With MCRA Global Access

Press Releases

MCRA Offers Informational Presentation on Medical Device Regulation to the Chinese FDA

MCRA Leads Innovation Training with FDA as Part of its Experiential Learning Program (ELP)

FDA Selects MCRA to Share Expertise as Part of the Experiential Learning Program (ELP)

MCRA Releases New White Paper Analyzing the Industry Impact of the Federal Budget Request on FDA

MCRA Advises Orthopedic Industry To Adopt Integrated Value Creation Strategy

MCRA Expands, Moves to New DC Location

SANUWAVE Health Submits de novo Petition for FDA Review and Classification of the dermaPACE System to Treat Diabetic Foot Ulcers

MCRA Assists Cartiva, Inc. with Obtaining FDA PMA Approval for the Company's Synthetic Cartilage Implant (SCI)

MCRA Assists VertiFlex, Inc. with Obtaining FDA PMA Approval for the Superion® Interspinous Spacer System

MCRA Hires Experienced Trauma And Total Joint Expert To Expand Its Leading Orthopedic Regulatory Team

MCRA Assists Wright Medical Group, Inc. with Obtaining FDA PMA Approvable Decision for Augment® Bone Graft