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What We Do Clinical Development

Clinical Development

Device-Focused Clinical Development, Built for Real-World Performance

Clinical development in MedTech is fundamentally different from pharma. Devices succeed or fail based on how they perform in real procedures, real workflows, and real clinical environments — not just controlled trial conditions. Evidence must reflect technique, usability, operator variability, and context, while still meeting rigorous regulatory expectations.

Avania’s clinical development model is purpose-built for medical technology. We integrate clinical operations, regulatory insight, data strategy, and device expertise into a single delivery model, ensuring studies generate evidence that is accurate, contextual, and ready for regulatory and commercial scrutiny. From early feasibility through post-market follow-up, we champion our sponsors’ programs with clarity, control, and confidence.

Explore Our Clinical Development Capabilities

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Clinical Development Capabilities

End-to-end clinical delivery for medical devices, diagnostics, and digital health — from first-in-human and pivotal trials through post-market surveillance. Integrated teams across project management, clinical operations, data, biostatistics, safety, and quality ensure evidence reflects real-world device use.

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Study Types

A full spectrum of MedTech study models, including early feasibility, IVD and diagnostic studies, pivotal trials, and post-market surveillance. Each study type is executed with operational models tailored to device workflow, technique, and use environment.

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Functional Service Partnerships (FSP)

Flexible, embedded expertise that scales with your program. Avania’s MedTech-focused FSP model provides dedicated support across clinical operations, regulatory affairs, quality, data, and medical writing, without sacrificing oversight or continuity.

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IVD & Diagnostic Studies

Precision-driven clinical programs for diagnostics, designed to align analytical performance, clinical validation, regulatory strategy, and market access. From feasibility through pivotal validation, studies are structured to withstand regulatory review and support adoption.

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Clinical Insight Embedded at Every Stage

Across every study type and engagement model, Avania integrates strategic advisory insight directly into clinical execution. Regulatory, engineering, and market access perspectives inform protocol design, operational decisions, and data strategy, helping avoid avoidable delays and ensuring evidence supports long-term approval and adoption.


Ready to Advance Your Clinical Program with

Confidence?

Move your device forward with a clinical development partner built for MedTech. Avania brings integrated clinical, regulatory, and operational expertise to help you plan, execute, and deliver high-quality evidence without losing sight of real-world performance.

Tell Us About Your Project