Clinical Services

End-to-end clinical research services to help biotechnology, pharmaceutical and medical device companies bring new drugs and devices to the market effectively and efficiently. We have expertise in working with sites and sponsors to break down silos and streamline processes.

Drug Safety Services

We provide clinical and post-marketing drug safety services, including end-to-end Case Processing, Aggregate Reporting, Clinical Safety Management, Signal Detection, Local PV Representation and audit support.

IRB Division

Sitero provides independent review committee solutions to ensure participants are protected and research is conducted in a responsible manner across all stages and therapeutic areas. Our services include IRB, IBC, DMC/DSMB and Biosafety consulting services.

Biosafety Services

Sitero handles the committee setup, protocol review, NIH registration, Risk Assessment, IBC charter and will guide the site and investigator through the review and approval process. Sitero handles all amendments and annual reviews.

Sitero Mentor Technology

The Sitero Mentor platform leverages intelligent automation to enable efficient reporting, communication and process management functions for research, Clinical and higher education institutions.