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Clinical researchProfessional or ₹2,400

ICH-GCP for Clinical Research

Good Clinical Practice as a working document rather than an exam topic: what the investigator owes, what the sponsor owes, and what a monitor is actually checking on a site visit. Certification is issued on completion.

6 hours12 lessonsNo prior industry experienceCertificate on completion
₹2,400one payment

Included in Professional at ₹499 a month, which works out cheaper at two courses or more.

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What it moves on your score
SkillsCareer-transition feasibilitySpecialty relevance
What you can do afterwards
Explain the thirteen principles without reciting them
Identify a protocol deviation and know who to escalate it to
Run source data verification against a case report form
Write a monitoring visit report that survives audit
Curriculum4 modules · 12 lessons
The framework
1Why GCP exists: Declaration of Helsinki to ICH E6Video12:00
2The thirteen principles in working languageVideo18:00
3Reference sheet: ICH E6(R2) principlesNotes
Who owes what
4Investigator responsibilitiesVideo16:00
5Sponsor responsibilities and delegationVideo14:00
6Ethics committee and informed consent in IndiaVideo17:00
Documents and data
7The trial master file, and what belongs in itVideo13:00
8ALCOA+ and why source data winsVideo15:00
9Reference sheet: essential documents checklistNotes
Monitoring
10What a monitor checks, in orderVideo19:00
11Protocol deviations: recognise, record, escalateVideo14:00
12Monitoring visit assessmentAssessment30:00
The first two lessons of every course are open. The rest need Professional.
Taught by
Dr. Rajesh Menon
Clinical operations lead, Nilgiri Biosciences

Fourteen years monitoring trials across India and Sri Lanka.

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