Maintain compliance with all established federal, state and local laws governing.

Regulatory review of essential documents, internal and external auditing as well as participation in audits, management of and surveillance program and regulatory consulting.

Provide reports on all initial study submissions, adverse events, protocol amendments, etc.

BRCR GLOBAL supports sites with submission of applications to their local OR central Institutional Review Board by providing Consent Form templates and other necessary documents, which may be customized to meet local requirements.


Boca Raton Clinical Research follows HIPAA Guidelines and maintains patient confidentiality. Patient registration, medical history, family history and trial participation is stored in our patient database and is never shared or sold