Global Regulatory, Product Development & Clinical Research Consultants
MDRS, LLC is an FDA registered company that specializes in providing strategic FDA and global regulatory, product development, quality and clinical research support to medical device and biotechnology companies and their development teams.
While MDRS specializes in providing global regulatory support to emergent medical device companies, the firm’s clientele include Fortune 500 biotechnology companies and leading Academic Medical Centers that have utilized the firm’s regulatory, clinical research and quality systems implementation and remediation services.
MDRS, LLC is a Founding Member of the NIH MPW REGENERATIVE MEDICINE RESOURCE CENTER: 2017-2025
MDRS provides comprehensive Total Product Life Cycle (TPLC) translational development consulting services to assist you in developing and maintaining high quality medical products for global markets. We help development teams navigate complex global regulatory requirements and share best practice methodologies associated with successful medical products development and commercialization. We provide regulatory, product development, quality and clinical research solutions at reasonable rates, so your team can afford early regulatory expertise to help your company develop high quality products with optimal efficiencies for long term success.
Our consulting team includes regulatory, product development, clinical, quality systems and commercialization experts with more than 170 years of combined experience developing and commercializing medical device, pharmaceutical and combination products.
President &
SVP, Regulatory & Clinical Research
SVP, Product Development
VP, Quality Engineering
Sr. Principal Consultant – Software Engineering
Sr. Principal Consultant – Commercialization
Abbott IVD
Airway Innovations
Alerje
Arbor Medical Innovations
Bodymatter
Cohera Medical
Danmar Products
Tangent Medical
The Patient Company
NeuroNexus
Navigate Surgical Technologies
NeuMoDx Molecular – Qiagen
Histosonics
Leica
Hygieia
Mar-Med
Microdermics
Navigate Surgical
Pixel / Ultrasound Medical Devices
IntroMedic
SpinTech
Sharp Laboratories
St. Blaise
Stemplant
Terran Biosciences
University of Michigan
Stanford University
Grand Valley State University
University of Pittsburgh – McGowan Institute for Regenerative Medicine
University of Washington
University of Louisville
University of California
Cleveland Clinic
Covenant Healthcare
Magee-Womens Research Institute & Foundation
Michigan State University
Norton Healthcare
Oregon Health Science University
Tufts University
Wayne State University
Washington University in St. Louis
University of Texas
Vanderbilt University
Wyss Institute – Harvard University
Taylor DP, Yoshida M, Fuller K, Giannobile WV, Sfeir CS, Wagner WR, Kohn DH. Translating Dental, Oral, and Craniofacial Regenerative Medicine Innovations to the Clinic through Interdisciplinary Commercial Translation Architecture. J Dent Res. Apr 27, 2021
Baman, TS, et al., Pacemaker Reutilization: An Initiative to Alleviate Symptomatic Burden Associated with Bradyarrhythmia in Impoverished Nations Around the World, AHA Circulation, October 19, 2010.
Support for Investigator-Initiated Clinical Research: The Clinical Translational Science Award (CTSA) Experience, Academic Medicine: February 2011 – Volume 86 – Issue 2 – pp 217-223; NIH-CTSA National IND/IDE Taskforce, co-author
Kaigler, D, Fuller, KL, Giannobile, WV, Regulatory Process for the Evaluation of Dental Drugs, Devices and Biologics In: Giannobile, WV, Burt, B, Genco, R. ed, Clinical Research in Oral Health, Wiley-Blackwell, released March 2010
National Cancer Institute: Network For Translational Research (NTR) Optical Imaging In Multimodal Platforms (U54): Year 1 Report: RFA-CA-08-002
MDRS, LLC
230 Collingwood Dr., Suite 260
Ann Arbor, MI 48103
Grand Rapids Satellite Office:
Doug Meijer Medical Innovation Building
Grand Rapids, MI 49503
Mon – Fri: 9AM – 5PM, EST
Sat & Sun: Closed
After Hours by Appointment Only
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