Description
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). 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).
Read More: www.thomasregulatory.com/
FDA masks and PPE Consultant FDA US Agent Consultant FDA COVID-19 Coronavirus SARS-COV-2 Consultant CER Consultant Clinical Evaluation Report Consultant 510k Consultant FDA Emergency Use Authorization EUA Consultant FDA medical device consultant EU CE Mark MDR Medical Device Consultant FDA Establishment Registration Medical Device Listing Consultants
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