Free Pharma Courses & Resources
Hand-picked free courses from WHO, CDISC, NIH, FDA, Coursera, Harvard and more. ClinPath curates the best — you learn for free.
Showing 29 courses
CDASH Fundamentals
CDISC
Learn the Clinical Data Acquisition Standards Harmonization (CDASH) model used globally in clinical trials. Covers domains, variables, and implementation.
SDTM Implementation Guide — Self-Study
CDISC
Master CDISC SDTM (Study Data Tabulation Model) standards used for FDA submissions. Free self-study resources and implementation guide walkthroughs.
Data Management in Clinical Research
SCDM
Introduction to clinical data management principles, tools, and processes. Perfect for freshers entering CDM roles at CROs and pharma companies.
ICH E6(R2) Good Clinical Practice (GCP)
ICH
Essential GCP guidelines every clinical data professional must know. Covers trial conduct, data integrity, and sponsor/investigator responsibilities.
Clinical Data Management Certificate Program
Coursera
Free audit available. Covers end-to-end CDM workflows including protocol review, CRF design, data validation, and database lock.
Pharmacovigilance — Basic Concepts
WHO-UMC
Free foundational course from the WHO global drug safety centre. Covers adverse drug reactions, signal detection, and pharmacovigilance systems.
Pharmacovigilance Master Class
EMA
EMA training covering pharmacovigilance legislation, PSUR/PBRER preparation, risk management plans, and ICSR reporting under EU regulations.
ICH E2E Pharmacovigilance Planning
ICH
Understand the ICH E2E guideline for pharmacovigilance planning. Essential reading for PV professionals working in global drug development.
Drug Safety and Pharmacovigilance
Coursera
Free audit option. Covers case processing, medical coding (MedDRA), causality assessment, and regulatory reporting timelines for ICSRs.
Introduction to Pharmacovigilance
OpenWHO
Completely free WHO course on pharmacovigilance fundamentals, the WHO Programme for International Drug Monitoring, and safety reporting systems.
Introduction to FDA Regulatory Science
FDA
Free FDA courses on drug development, approval processes, IND/NDA/BLA submissions, and regulatory science fundamentals in the US market.
ICH Guidelines Overview (Q, S, E, M series)
ICH
Comprehensive coverage of ICH quality, safety, efficacy, and multidisciplinary guidelines. Essential for regulatory affairs professionals.
Regulatory Affairs Fundamentals
RAPS
RAPS free resources covering RA career paths, global regulatory frameworks, and regulatory strategy for pharmaceutical and medical device products.
WHO Prequalification Training
WHO
WHO training on prequalification of medicines, quality standards, and dossier submission for global health markets. Critical for RA in generics.
SAS Programming 1 — Essentials
SAS Institute
Official free SAS programming course covering DATA step, PROC SQL, and basic macros. The #1 starting point for pharma SAS programmers.
Introduction to Clinical SAS Programming
PharmaSUG
Clinical trial data programming using SAS. Covers CDISC SDTM mapping, ADaM datasets, and TFL (Tables, Figures, Listings) generation for pharma studies.
SAS OnDemand for Academics — Free Platform
SAS Institute
Completely free SAS software in the cloud for students. Practice SAS programming with real datasets. No installation required — start immediately.
R Programming for Clinical Trials
Johns Hopkins
Free audit available. R is rapidly replacing SAS in pharma. This course covers data manipulation, statistical analysis, and visualisation for clinical data.
Biostatistics in Public Health
Johns Hopkins
Free audit available. Covers descriptive statistics, probability, hypothesis testing, regression, and survival analysis in clinical trial contexts.
Statistics for Clinical Trials
Harvard MRCT
Harvard's Multi-Regional Clinical Trials Center free training on statistical concepts for clinical trial design, sample size, and analysis plans.
Introduction to Statistics with Python
UMich / Coursera
Free audit. Python is increasingly used in pharma biostatistics. Learn statistical analysis, data visualisation, and hypothesis testing using Python.
Good Clinical Practice (GCP) Certification
NIH
Free NIH GCP training widely accepted by sponsors and CROs. Essential for Clinical Research Associates (CRAs) and anyone working in clinical trials.
CITI Program — Clinical Research Training
CITI Program
The most widely-required training for clinical research professionals. GCP, human subjects research ethics, and site monitoring covered. Free for many institutions.
Clinical Trial Management Fundamentals
ACRP
Free ACRP resources on clinical trial management, site operations, protocol deviations, and the role of CRA in sponsor oversight.
Introduction to Clinical Trials
Duke / Coursera
Free audit available. Covers clinical trial phases, protocol design, randomization, blinding, site management, and data quality in clinical operations.
CCDM Exam Preparation Resources
SCDM
Official SCDM resources for the Certified Clinical Data Manager (CCDM) exam. Study guides, Good Clinical Data Management Practices (GCDMP) reference, and exam blueprints.
CCDS — Drug Safety Certification Prep
DIA
Preparation resources for the Certified Clinical Data Scientist (CCDS) exam — covers pharmacovigilance, data science, and regulatory reporting for PV professionals.
RAC Certification Study Resources
RAPS
Free RAPS study materials for the Regulatory Affairs Certification (RAC). Covers global regulatory strategy, submissions, and lifecycle management.
ACRP Certified Clinical Research Coordinator (CCRC)
ACRP
Certification prep for CCRC and CCRA credentials. Free study guides, practice questions, and eligibility requirements from ACRP.
ClinPath does not create any of these courses. We curate and surface the best free resources from trusted organisations — WHO, CDISC, NIH, FDA, Coursera, Harvard, and more — so you don't have to spend hours searching. All links open on the original provider's website.