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FDA Quality and Regulatory Consultants was founded in 2009 with the long-term goal to provide sound scientific and technical expertise in quality assurance, regulatory affairs and compliance to our pharmaceutical, medical device and biotech clients from the laboratory, across human trials, to the manufacturing environment, and beyond to marketing approvals globally.  Our dedicated team of professionals strive to provide risk based assessments focusing on the health and welfare of the global population while minimizing the regulatory risk for our clients.  We use three (3) elements when conducting projects; Process, Paper and People. 


Providing outstanding consulting services is our highest priority. We bring a technical expertise to all our projects while providing high-quality deliverable. We also seek to help our Consultants perform meaningful work that will make the most of their advanced skills. FDAQRC has two (2) customers Clients and Consultants. We strive to offer our Consultants meaningful projects making the most of their advanced expertise.   Utilizing our proprietary tool, FDAQRConnect, we leverage our detailed knowledge of our consultants to provide the right consultant to the client for each project.

FDAQRC holds true to the core values of integrity, loyalty, ethical business practices and treating our customers with the utmost respect.  We want to be your Quality and Regulatory Consultants, now and in the future.

Availability for Work


Area(s) of Expertise

GLP, GMP, GCP, Field Studies, PV, Computing, GCLP, Non-Reg Research, Specialising in ex-FDA Inspector Consulting and Response Support

Contact Details

Chris Rush, President

100 E Whitestone Blvd, Suite 148-262

Cedar Park, TX78613


Tel: +1 (214) 529-0248

Email: info@fdaqrc.com

website: www.fdaqrc.com

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