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About Us

TRR is a consulting firm in the Quality, Quality Management Systems, Regulatory Affairs, Global Regulatory Submissions (including FDA and European CE Mark) and Compliance (Audit Preparation, Audit Training, Audit Support, Internal Auditing) Space specializing in the medical device space, general manufacturing space, and life sciences space (Bio-medical and Bio-Pharma).

How We Got Started

TRR was founded on the principles of providing LEAN regulatory and quality and auditing support to the industry at a competitive rate in order to get client products to market quicker and get ISO certification quicker (ISO 9001 and ISO 13485).

Our Ideal Customer

Medical Device Manufacturers, Start-up Med Device Companies, General Manufacturing Companies, Lifesciences Companies, Pharma, Biotech, Cosmetics Manufacturers, located in any location. TRR is available to travel domestically (US) and abroad as clients may need.

Our Team
Dallas L. Thomas, RAC, MHA, MPA, Certified Lead Auditor, SSYB from Thomas Regulatory Resolutions
Dallas L. Thomas, RAC, MHA, MPA, Certified Lead Auditor, SSYB
President and CEO
Products & Services

Regulatory Submission Strategy and Quality Assessments

Do you have a global regulatory submissions plan that includes FDA (510k or Pre-Sub or Pre-IDE), European Union CE Mark, Health Canada Licenses, Asia submissions, Latin America Submissions, Middle East Submissions? We can provide an assessment for your company.

Quality Auditing, Audit Prep, and Audit Support

We conduct internal quality systems audits to find any gaps and ensure your quality system is robust. We also train for external audit preparation (ISO, Notified Body, FDA, ANVISA, Etc.) If you need on site support during your audit we also offer this service as well.
Businesses We Recommend
Nelipak does a great job in the life sciences packaging space. Definitely recommend.
WCS was great to work with for getting consular legalization and apostille for FDA issued documents for our medical device submissions to ministries of health around the world as well as authentication of original documents. Very reliable service over the nearly 4 year experience I have working with them.
Aegis Regulatory Consulting is a highly skilled professional firm. Great to work with.
Coweta MedTech Partners are highly skilled professionals who are great to work with.
Top Forum Activity
Dallas L. Thomas, RAC, MHA, MPA, Certified Lead Auditor, SSYB answered As A Consultant, What's Your Favorite Project Management...
4 months ago
I do regulatory affairs, quality, compliance, and auditing for the medical device industry and life sciences industry. I really like to use Asana. It offers enough functionality for an independent... (more)
Dallas L. Thomas, RAC, MHA, MPA, Certified Lead Auditor, SSYB reviewed Apple Ratings and Reviews
12 days ago • 1 Reply
Pros: Apple nowadays has pretty much the same functionality of Windows PC with fewer bugs/glitches/viruses in my experience. Also, the visuals are great. The speed is also awesome on Mac. I have... (more)

Highly Recommended

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