Advanced Programs

The Advanced Diploma in Clinical Research & Pharmacovigilance (ADCR-PV) covers the core areas of the Clinical research and Pharmacovigilance processes and equips you to start a career as a Clinical Research or Drug Safety professional. The course is aligned to the requirements of the industry and imparts clinical research and pharmacovigilance process knowledge in a clear and concise manner so that you may kickstart a career in clinical research and pharmacovigilance. This program includes hands-on training modules on Oracle Siebel Clinical - CTMS for Clinical Research and Oracle Argus Safety for Pharmacovigilance.

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The Advanced Diploma in Clinical Research & Data Management (ADCR-DM) is designed to provide students a complete understanding of clinical research and clinical data management processes. It equips you to start a career in Clinical Research Operations or as a Clinical Data Management professional. The course is aligned to the requirements of the industry and  includes hands-on training modules on Oracle Siebel Clinical - CTMS for Clinical Research and Oracle Clinical - CDMS for Clinical Data Management.

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The Advanced Diploma in Clinical Research & Medical Writing (ADCR-MW) is designed to provide you a complete understanding of the core areas of clinical research and medical writing. It equips you to start a career in Clinical Research Operations or as a Medical Writer. The course is aligned to the requirements of the industry provides comprehensive knowledge of all aspects of the curriculum.

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The Advanced Diploma in Clinical Research & Regulatory Affairs  (ADCR-RA) is designed to provide you a complete understanding of the core areas of clinical research and pharmaceutical regulatory affairs. It provides knowledge of global regulatory framework and develops skills required for regulatory strategy planning to ensure regulatory compliance. The course is aligned to the requirements of the industry and prepares you for the role of a regulatory affairs specialist for pre and post marketing studies.

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The Advanced Diploma in Pharmacovigilance & Data Management (ADPV-DM) is designed to provide students a complete understanding of Pharmacovigilance and Clinical Data management processes, regulations and documentation. It equips you to start a career in Drug Safety or as a Clinical Data Management professional. The course is aligned to the requirements of the industry and  includes hands-on training modules on Oracle Argus Safety for Pharmacovigilance and Oracle Clinical  for Clinical Data Management.

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The Advanced Diploma in Pharmacovigilance & Medical Writing (ADPV-MW) is designed to provide students a complete understanding of Pharmacovigilance processes, regulations and documentation as well as equip you with the skills required for writing clinical study reports as well as various clinical trial, regulatory and other scientific documents . It equips you to start a career in Drug Safety or as a Pharmaceutical Medical Writer. The course is aligned to the requirements of the industry and includes hands-on training modules on Oracle Argus Safety for Pharmacovigilance.

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The Advanced Diploma in Pharmacovigilance & Signal Detection (ADPV-SD) is designed to provide students a complete understanding of Pharmacovigilance and Signal Detection processes, regulations and documentation. It equips you to start a career in Drug Safety or as a Pharmacovigilance Signal Detection professional. The course is aligned to the requirements of the industry and  includes hands-on training modules on Oracle Argus Safety for Pharmacovigilance and Oracle Empirica Signal for Signal Detection.

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The Advanced Diploma in Pharmacovigilance & Regulatory Affairs (ADPV-RA) is designed to provide students a complete understanding of Pharmacovigilance processes, regulations and documentation as well as the pharmaceutical regulatory affairs landscape. It equips you to start a career in Drug Safety or as a Regulatory Affairs specialist. The course is aligned to the requirements of the industry and includes hands-on training modules on Oracle Argus Safety for Pharmacovigilance.

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The Advanced Diploma in Regulatory Affairs & Medical Writing (ADRA-MW) is designed to provide students a complete understanding of clinical trial regulations, regulatory documents created during the clinical trial process and tasks of performing medical writing for these documents. It equips you to start a career in Regulatory Affairs specialist or as a Medical writer. The course is aligned to the requirements of the industry.

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