Dallas L. Thomas, RAC, MHA, MPA, Certified Lead Auditor, SSYB
Thomas Regulatory Resolutions
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).
Recommendations Received (18)
"Very competent and pleasant to work with."
"I have been networking with Dallas for several years! With his background in Regulatory and..."
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"I have been networking with Dallas for several years! With his background in Regulatory and Quality Affairs you cannot go wrong bringing him on to your team. A well balanced set of qualifications to support all areas of your quality systems. "
Products & Services
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, As...
We conduct internal quality systems audits to find any gaps and ensure your quality system is robust. We also train for external audit preparation ...
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Recommendations Given (77)
"Reino has great experience in Engineering in the medical device industry. "
"Orlando and his team are highly competent in Quality work for clients! I have been working with..."
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"Orlando and his team are highly competent in Quality work for clients! I have been working with Orlando for a number of years and VQC is always very competent and professional. Highly recommended. "
Recent Activity
Yes, very much worth it to transfer to the ISO 9001:2015.
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Yes, very much worth it to transfer to the ISO 9001:2015.
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 consultant or for group tasks and projects. I have been using Asana now for over 3 years. They offer...
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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 consultant or for group tasks and projects. I have been using Asana now for over 3 years. They offer a free and a paid version. Both of which have great functionality. Check it out at www.asana.com . Happy to help out where I can if anyone ever wants to reach out and PM me or connect here on Alignable. I love to pay it forward where I can.
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 had less issues with my Mac than with PC (less crashing, etc). Microsoft Office works great and is...
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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 had less issues with my Mac than with PC (less crashing, etc). Microsoft Office works great and is totally compatible with the PC version when you need to jump back and forth. Also Facetime on my macbook is nice to have a direct way to talk with those with Iphones and Macs.
Cons: Price....Macs are much more expensive. The keyboard and shortcuts can take some getting used to, but other than that it is pretty user friendly and very straightforward.
I do regulatory affairs, quality, and compliance in the medical device field. Feel free to connect with me and PM me if I can help with any questions. I may be able to point you to the right person if you have specific questions as I have been in the med device field for a number of years and...
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I do regulatory affairs, quality, and compliance in the medical device field. Feel free to connect with me and PM me if I can help with any questions. I may be able to point you to the right person if you have specific questions as I have been in the med device field for a number of years and have a variety of connections.