Our Programmes

PG Diploma in Clinical Research

Comprehensive training in clinical trials and research operations.

Medical Writing – Drug

Scientific and regulatory writing for pharmaceutical research.

Medical Writing – Medical Device

Regulatory documentation aligned with EU MDR and FDA.

Regulatory Affairs

Global regulatory submissions and compliance training.

Pharmacovigilance

Drug safety, case processing, and signal detection.

Clinical Data Management

EDC systems, CRF design, and CDISC standards.

Clinical SAS

SAS programming for clinical trials and submissions.