The Clinical Research Team at Pharmazone is responsible for overseeing and managing clinical trials to ensure they are conducted in compliance with Good Clinical Practice (GCP) guidelines. This involves activities such as study design, clinical monitoring, auditing, and project management for bioequivalence and late-phase studies. The team collaborates with contract research organizations (CROs), manages clinical research associates, facilitates GCP audits, and supports the setup and upgrading of clinical research operations. Their work ensures the successful execution and regulatory compliance of clinical trials, contributing to the efficient development of pharmaceutical products.
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