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). For more information visit :
