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Webinar - From scoping to systematic: Choosing the right literature review for your evidence needs
On Tuesday, 6 October 2026, Genesis Research Group's evidence synthesis, HEOR, and evidence planning teams will be presenting a webinar in partnership with online real-world evidence and HEOR research hub The Evidence Base. The topic of the webinar is 'Fr
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What is regulatory-grade RWE?
Quick answer: What makes real-world evidence regulatory-grade? Regulatory-grade real-world evidence (RWE) is evidence generated from real-world data (RWD) in a way that can withstand regulatory, HTA, or payer scrutiny. It is not created by using a large o
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How the FDA uses real-world evidence in regulatory decisions, and what has changed since 2023
First published: 11 October 2023 Updated: 21 September 2026 The FDA accepts real-world evidence (RWE) in regulatory decision-making for drugs, biologics, and medical devices, but only when the underlying real-world data (RWD) source has been evaluated as
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Genesis Research Group Appoints Sarah Alwardt, PhD, as Executive Vice President, RWE/HEOR
11 August 2026 - Genesis Research Group today announced the appointment of Sarah Alwardt, PhD, as Executive Vice President, RWE/HEOR. She joins the Executive Leadership Team and will lead the company's global real-world evidence (RWE) and health economics
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The False Confidence of Unanchored MAICs: Lessons in Ulcerative Colitis
Methodological & Statistical Research This poster compares anchored and unanchored matching-adjusted indirect comparisons (MAICs) using Phase III trial data in moderate-to-severe ulcerative colitis. The analysis evaluated how each approach influences esti
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Early perspectives on health technology assessment in the Kingdom of Saudi Arabia: exploratory survey into market access implications
Health Technology Assessment As the Kingdom of Saudi Arabia (KSA) implements new health technology assessment (HTA) requirements, understanding how economic evaluations may influence future pricing and reimbursement decisions is becoming increasingly impo
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US Payer Perspectives on Drug Manufacturer Readiness for Artificial Intelligence
Organizational Practices As AI becomes increasingly integrated into healthcare decision-making, understanding payer expectations is critical. This poster explores US payer perspectives on drug manufacturer readiness for AI, finding that while payers are r
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A Modular Oncology Reference Model for Early Economic Evaluation: A Case Study in EGFR-Mutated NSCLC
Methodological & Statistical Research In oncology HEOR, the methodological choices behind a cost-effectiveness estimate can shape decisions long before mature clinical data are available. This poster presents a modular oncology reference model for early e
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The Institute for Clinical and Economic Review (ICER) Assessment Approaches to Survival Extrapolation: A Review and Case Study
Methodological & Statistical Research Looking back and pressure-testing the assumptions behind oncology cost-effectiveness evaluations. This poster reviews how ICER selected survival-extrapolation curves across oncology assessments between 2016 and 2025.
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Hoboken
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Hoboken, US (Headquarters)
200-500 est. staff
111 River Street, Suite 1120, Hoboken, 07030
