STUDY SUPPORT

Reporting serious adverse events to the Sponsor or CRO and the IRB/IEC.


Advising & alerting investigators of potential protocol violations.


Advising & alerting investigators of potential ICH-GCP violations.


BRCR GLOBAL provides continuous support to all the study personnel throughout the trial to guarantee a rapid learning curve and improve protocol adherence.

Project managers maintain close contact with sites for issues concerning to the study’s conduct, while data managers handle data queries and verification.

BRCR GLOBAL can also provide a 1-800 Help Desk through an experienced project manager or medical advisor, who are able to respond and assist to any queries from investigators and subjects.


PATIENT REGISTRATION

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