Advanced Diploma in Clinical Research

TThe Advanced Diploma in Clinical Research is a 12-month specialized program designed to provide comprehensive knowledge and practical skills required in the pharmaceutical, biotechnology, and healthcare industries. This program covers key areas such as clinical trial management, regulatory affairs, pharmacovigilance, medical writing, and clinical data management (CDM).

With an industry-driven curriculum and hands-on internship experience, this course equips students with the expertise needed to excel in the fast-growing field of clinical research.

Course Highlights

Fundamentals of Clinical Research & Clinical Operations

Learn about clinical trial design, protocols, and ethical considerations.
Gain insights into Good Clinical Practice (GCP) and regulatory compliance.

Regulatory Affairs

Understand global regulatory guidelines
Learn submission processes and drug approval requirements.

Medical Writing

Develop skills in writing clinical trial reports, regulatory documents, and scientific publications.

Clinical Data Management (CDM)

Gain practical knowledge of data collection, database design, validation, and analysis.

Pharmacovigilance

Learn about drug safety monitoring, adverse event reporting, and risk management.

Statistics in Clinical Research

Apply biostatistical methods for clinical data analysis and decision-making.

Advanced Diploma in Clinical Research

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