Orbis Clinical offers a variety of services for clients and consultants, which includes:

Regulatory Affairs: Our regulatory affairs practice has dedicated resources to meet the mission critical and often timely challenges our clients face.

Medical Affairs: Our Medical Affairs division has experienced personnel who can educate department members, see that consumer questions are addressed, provide input and expertise in the design and construction of all promotional materials and events, and provide informational services to health care providers in the community.

Medical Writing: Orbis Clinical’s medical writing practice provides our clients with experienced, knowledgeable professionals to properly address all facets of clinical and post marketed communication.

Quality Assurance: Orbis Clinical has the quality assurance expertise to assist pharmaceutical and biotechnology firms with auditing and improvements relative to Good Clinical Practices/GCP, Good Laboratory Practices/GLP, and Good Manufacturing Practices/GMP.

Drug Safety: Our consultants can provide the expertise to assist in the development and management of your clinical and post marketed safety programs to ensure patient safety through efficient and effective processes.

Clinical Research: Orbis Clinical supports the evolving clinical research industries by providing flexible staffing solutions to grow, develop, and manage your clinical trials. We assist with providing professionals at Medical Device companies, CRO's, Biotech/Pharmaceutical, Universities, Hospitals and Research sites.


 

To learn more about our services, contact us today!

Toll Free: 1-866-879-1963

Phone: 781-569-0607

Fax: 866-915-6480

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