Our Services

Management of clinical projects in support of Global R&D Clinical Trials and other supportive research and development needs. This includes coordination and management of clinical studies, vendors, CROs, drug product supply, blinding, packaging, labeling, and distribution activities of Investigational Medicinal Products (IMP).escription text goes here

Our GMP Auditors provide third-party verification that good manufacturing practices (GMP) are followed. These practices ensure that products are manufactured consistently to an expected level of quality. They are also required to conform to regulatory agency recommended guidelines.

• Internal facility audit to help prepare your company or contractor for FDA inspection

• Packaging/labeling contractors

• Warehouses

• Distribution Centers