Launch & Commercialization

Medical device launch and commercialization

Cetas Healthcare’s Launch & Commercialization services help MedTech companies translate clinical value into market value. We support you from pre-launch through expansion with evidence-driven insights that strengthen positioning, accelerate adoption, and build sustainable market traction.

Our Offerings

Value Proposition & Message Testing

Develop, refine, and validate clinical, operational, and financial value stories that resonate with target customers.

Segmentation Research (STP Framework)

Identify priority customer segments and position your product to meet distinct needs across specialties, facility types, and patient groups.

Pricing & Market Access

Use robust pricing methodologies to determine willingness-to-pay, optimize pricing strategy, and strengthen your product’s reimbursement potential.

KOL Engagement

Identify, recruit, and engage key opinion leaders to support evidence generation, clinical validation, advisory boards, and market influence.

Case Studies

Pricing Research for Electronic Data Concept for Cell Culture Media
Biopharma

Pricing Research for Electronic Data Concept for Cell Culture Media

Pricing research was conducted with 160 biopharma stakeholders to assess interest, needs, and willingness to pay for a new electronic data concept for cell culture media. The study identified key challenges.

Value Proposition and Message Testing – Interventional Technologies
Interventional Technologies

Value Proposition and Message Testing – Interventional Technologies

Stakeholder research across US/EU specialists tested three value propositions for a new IXR solution, uncovering unmet needs, workflow challenges, and purchase likelihood to refine and strengthen messaging.

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Contact Our MedTech Experts

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Certification 1ISO 9001ISO 14155GDPR

Cetas Healthcare is the world’s leading boutique MedTech market research firm. We blend agency-grade research with strategic intelligence frameworks to track pipelines, regulatory shifts, clinical trials, and GTM strategies. As pioneers of ISO 14155-compliant PMCF surveys, we’ve managed 25,000+ patient case forms for Class II & III devices, helping clients secure CE certifications and stay ahead of EU MDR requirements.