Thomas Regulatory Resolutions, Inc. / TRR

medical devices

About

Thomas Regulatory Resolutions (TRR) is a lean medical device consulting firm serving the medical device industry by providing value-added consulting services to medical device manufacturers for FDA submissions, FDA Compliance, FDA 510(k), Establishment Registration, FDA US Agent, CE Marking per EU MDR 2017/745 and Clinical Evaluation Reports (CERs) among other regulatory services to medical device manufacturers Count on us for all of your medical device regulatory submission needs. You may contact us via phone at +1 561 898 0260 or email our office to [email protected] or if you are ready now to schedule a free 30 minute appointment with us, please do so here: https://thomas-regulatory.appointlet.com and we are standing by to support your medical device regulatory submission needs. Also check us out at www.thomasregulatory.com #medicaldevice #510k #fda #regulatoryconsultant #510kconsultant #fdaconsultant #medtech #meddevice #EUMDR #CEMark #CER #MEDDEV

Technologies

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Keywords

regulatory affairs iso 13485 fda auditing 510 pma ce mark medical device anvisa us agent medical device regulation regulatory consultant internal quality management system audit cer europe latin america portuguese spanish regulatory compliance life sciences biopharma brazil medical device single audit program mdsap 21 cfr 820 quality systems regulation fda florida mdsap meddev 27 1 rev 4 fda us agent

Location

5613 Tiger Way, Winter Garden, Florida, United States, 34787-5683

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