Clinical Research Consulting & Staffing
In an environment of rapidly evolving regulatory standards it is critical for biopharmaceutical companies to stay current with mandatory regulatory reporting requirements and industry best practices.
Orbis Clinical provides comprehensive drug safety consulting services exclusively. Orbis’ professional services expertise includes risk management and assessment, clinical and post marketed drug safety, and pharmacovigilance.
Expertise includes, but is not limited to, case initiation, narrative writing and case processing, individual case review, aggregate data review, signal detection, ad hoc safety reports, PSUR, label review, risk mitigation and action plans, litigation case processing, and medical writing.
For more information on Orbis’ services, visit www.orbisclinical.com.