Evidence that drives access, reimbursement, and value.
We unify HEOR, RWE, biostatistics, and HTA expertise to design evidence strategies that meet payer and clinical expectations. Our work spans planning, generation, and communication, ensuring value is supported across markets and lifecycle stages. With experience in major global HTA processes, we equip clients with evidence that drives access and strengthens competitive positioning.
Eric is a global executive in evidence development, value demonstration, access, and commercialization with 25+ years of experience. A recognized thought leader in emerging technology evidence, he has supported 750+ peri- and post-approval scenarios.
Catriona leads Putnam’s health economic modelling team, specializing in global and HTA-focused models. She has developed models across oncology, chronic diseases, and rare conditions to support rigorous value assessment and payer decisions.
Sylvaine leads data analytics within the VPA team and oversees RWE projects, focusing on evidence synthesis and claims database analysis. She develops innovative analytical methods to produce insights from large, complex datasets.
Yemi leads the patient-reported outcomes and preference elicitation team, partnering with clients to translate patient insight into impactful evidence generation, underpinned by deep scientific expertise in quality-of-life measurement and valuation with extensive HTA experience across a wide range of therapeutic areas.
Clement leads the HTA and Market Access Operations team, advising biopharma from early asset planning through launch. He brings deep HEOR, HTA, and market access experience, including 15 years leading global HEOR teams in industry.
Simon is a seasoned market access leader advising clients from asset strategy through peak sales. He has delivered numerous HTAs, negotiations, and pricing strategies across hematology, oncology, ophthalmology, neurology, and rare diseases.
Yoshie manages Japan-focused projects including database analysis, cost-effectiveness studies, clinical outcome assessment, and HTA submissions. Her expertise spans biostatistics, epidemiology, healthcare policy, and pharmaceutical market access.
Erika helps clients develop strategies for pipeline agents, assess commercial opportunities, and address access topics across oncology, vaccine-preventable diseases, immunology, neurology, and rare diseases.
Lori’s expertise spans stakeholder engagement, center-of-excellence profiling, organizational design, strategic medical launches, integrated evidence planning, omnichannel strategy, and digital health platforms including digital therapeutics, AI, and software as a medical device.
Access the most up-to-date health and life sciences insights and resources.
Key insights from ISPOR Europe 2025 on evolving HEOR, RWE, AI-driven evidence, patient-centered outcomes, and the future of market access.
Discover how real-world external control arms (RW-ECAs) provide robust comparative evidence for HTA submissions when RCTs are impractical or unethical
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