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DRUG DEVELOPMENT
GCP Foundations
Core principles of Good Clinical Practice (ICH E6) including investigator responsibilities, informed consent, monitoring, and regulatory inspection readiness. Suitable for professionals entering clinical research or consolidating foundational knowledge.
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IN DEVELOPMENT
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5 programmes
The following programmes are currently in development. Register your interest to be notified as soon as enrolment opens.
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PRECISION MEDICINE
Companion Diagnostics (CDx)
Regulatory frameworks, clinical co-development strategy, and biomarker validation for CDx programmes aligned with FDA and EMA guidance.
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AI & TECHNOLOGY
AI Literacy for Pharma Professionals
Foundational understanding of machine learning, large language models, and AI applications across drug discovery, development, and regulatory submissions.
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DRUG DEVELOPMENT
Decoding Drug Modalities
A comparative overview of small molecules, biologics, cell and gene therapies, oligonucleotides, and antibody-drug conjugates — covering mechanisms, development challenges, and regulatory pathways.
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DRUG DEVELOPMENT
Real-World Evidence in Drug Development
Design and interpretation of real-world studies, regulatory expectations for RWE in labelling and post-approval contexts, and use of electronic health records and registries.
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DRUG DEVELOPMENT
Clinical Trial Design Foundations
Core principles of clinical trial design including phase structures, randomisation, blinding, endpoints, sample size considerations, and ICH E8/E9 alignment. Suitable for professionals entering clinical development or consolidating foundational knowledge.
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The curriculum is shaped by the needs of professionals working in pharmaceutical development. If a topic is missing, the suggestion is taken into account when planning future programmes.
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