Enhancing the Biotechnology Industry
with HEOR

We support clients in the development, execution, and dissemination of the clinical
and economic evidence to ensure effective patient access.

Our clients are dedicated to developing life-saving innovations for patients who need them most, and we’re committed to supporting their evidence generation journey. The right health economic & outcomes research (HEOR) support can not only accelerate go-to-market efforts for the best innovations – it can break down barriers to patient access and communicate value to private and public payers. 

How Can We Help?

We empower our clients with the data and insights to establish your value narrative. Through our HEOR services, we support clients in the development, execution, and dissemination of the clinical and economic evidence to ensure effective patient access to life-saving treatment in the biotechnology space.

Our team of experienced health economists, epidemiologists, and data scientists have significant experience in applying advanced economic methods to effectively capture all dimensions of value of healthcare innovations. We work with our clients to ensure that the manufacturers effectively communicate value and maximize patient access.

Our services also include high-level support for responding to ICER reviews and health technology assessments for US-based and international clients, to optimize performance and increase the likelihood of approval.

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Our HEOR services include but are not limited to:

Pre-approval

Post-approval

Strategic evidence generation plans
Burden of Illness and cost of illness studies
Early cost-effectiveness modeling and scenario analysis
Quantification of market size and unmet medical need
Identification of outcome research endpoints​
Cost-effectiveness analysis alongside clinical trials
Patient-reported outcomes
Support for ICER and HTA reviews
Budget impact models
Economic evaluation
Real-world evidence generation plans
Real-world evidence studies
Payer engagement support

Our HEOR services include but are not limited to:

Pre Approval

Phase 1 - Phase 3

Strategic Evidence Generation Plans

Phase 1 - Phase 3

Burden of Illness and cost of illness studies

Phase 1 - Phase 2

Early cost-effectiveness modeling and scenario analysis​

Phase 1 - Phase 2

Quantification of market size and unmet medical need

Phase 2 - Phase 3

Identification of outcome research endpoints​

Phase 2 - Phase 3

Cost-effectiveness analysis alongside clinical trials

Phase 3

Patient-reported outcomes

Phase 4

Support for ICER and HTA reviews

Phase 4

Budget impact models

Phase 4

Economic evaluation

Phase 4

Real-world evidence generation plans

Phase 4

Real-world evidence studies

Phase 4

Payer engagement support

Post Approval

Phase 4

Strategic Evidence Generation Plans

Phase 4

Burden of Illness and cost of illness studies

Phase 4

Patient-reported outcomes

Phase 4

Support for ICER and HTA reviews

Phase 4

Budget impact models

Phase 4

Economic evaluation

Phase 4

Real-world evidence generation plans

Phase 4

Real-world evidence studies

Phase 4

Payer engagement support

Stage Analytics
Stage Analytics

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