About MediKnowl
MediKnowl is a modern learning management platform engineered by Mediception to empower organisations, educators and learners across the clinical research, MedTech and pharma landscape. We combine robust technology, scalable architecture and intuitive design with faculty who have run trials, filed submissions and been audited.
Compliance as the baseline
Content is reviewed against ICH-GCP E6(R3), NDCT Rules 2019, Schedule Y, 21 CFR Part 11 and EU CTR 536/2014.
Role-based curriculum
Each programme is mapped to a real job description — CRA, CRC, RA associate, drug safety officer, data manager, medical writer.
Global + India context
CDSCO, US FDA and EMA pathways taught side by side so learners can work on multi-region trials.
How the platform is governed
Clinical trial teams are audited, so their training platform should behave like a controlled system. These are the practices we hold ourselves to.
- Curriculum reviewed by practising clinical research professionals
- Case studies drawn from real (de-identified) trial scenarios
- Assessments graded by faculty, not auto-scored quizzes only
- Version-controlled content with dated updates on regulatory change
- Learner records retained with completion timestamps for audit
- Module-level access control so sponsors can scope training precisely
For sponsors, CROs and sites
Onboard a whole study team, assign only the modules a role requires, monitor completion in the admin console, and export a training log when an inspector asks for it.
Discuss cohort training