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 Lauren@thomasregulatory.com 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