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Health Technology Assessment (HTA) Masterclass

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How drugs get evaluated for pricing and reimbursement: agencies, dossiers, cost-effectiveness, and real case studies
1
1/5
(66) Ratings
104 students
Created by David LL.
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What you'll learn

  • Explain what health technology assessment is and why payers rely on it
  • Navigate the HTA process from dossier submission to reimbursement decision
  • Compare the major HTA agencies: NICE, HAS, IQWiG/G-BA, Canada’s Drug Agency, INESSS, ICER, PBAC, and more
  • Read and critique an HTA dossier: PICOS, clinical evidence, indirect comparisons
  • Understand QALYs, ICERs, cost-effectiveness thresholds, and economic models in plain English
  • Evaluate budget impact and uncertainty analysis like an agency reviewer
  • Explain managed entry agreements, reference pricing, and tendering
  • Apply HTA thinking through realistic oncology, rare disease, and vaccine case studies
  • Map the careers in HTA and market access — and plan your entry with a first-90-days playbook
This course includes:
2.5 total hours on-demand video
0 articles
0 downloadable resources
40 lessons
Full lifetime access
Access on mobile and TV
Certificate of completion
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Course content

Requirements

  • No prior HTA or health economics background needed — this course starts from zero
  • Curiosity about how drug pricing and reimbursement decisions get made

Description

This course contains the use of artificial intelligence.

Every drug that reaches patients has passed through a second, invisible trial: health technology assessment. HTA agencies decide whether a medicine is worth its price — and their verdicts determine which drugs get reimbursed, which get restricted, and which never launch. This course teaches you how that system actually works, created by instructor David LL and brought to life with professional AI production tools.

You’ll start with the fundamentals: what HTA is, why payers need it, and how the assessment process runs from submission to decision. Then you’ll tour the agencies that shape global markets — Canada’s Drug Agency and INESSS, the UK’s NICE and SMC, France’s HAS, Germany’s IQWiG and G-BA under AMNOG, plus the key players in Italy, Spain, the Nordics, Benelux, the United States, Australia, Brazil, and Japan.

Then it gets technical in the best way. You’ll learn how HTA dossiers are built — PICOS framing, clinical evidence requirements, indirect comparisons and network meta-analysis — and how economists measure value: QALYs, the incremental cost-effectiveness ratio, willingness-to-pay thresholds, economic models, budget impact, and uncertainty analysis. You’ll see how recommendations turn into prices through managed entry agreements, international reference pricing, and tenders.

Finally, you’ll apply it all through realistic case studies — an oncology drug at NICE, a rare disease therapy, a vaccine decision, and what happens when HTA says no — before a dedicated careers section shows you the jobs in HTA and market access, the skills that get you hired, and your first-ninety-days plan for breaking in.

No prior HTA experience needed. No equations, no jargon walls. Just a clear, practical understanding of how medicines earn their price — and how you can build a career in the field.

Who this course is for:

  • Pharma and biotech professionals who work with — or around — market access, pricing, and reimbursement
  • Job seekers targeting HTA, health economics, outcomes research, or market access roles
  • Students of pharmacy, public health, or health policy who want practical, career-ready knowledge
  • Anyone who finished a market access course and wants the natural sequel: how value gets proven
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