Solutions

The exact level of clinical support you need today.

Whether taking full ownership of your trial, managing specific functional areas, or integrating expert talent directly into your team. You define the collaboration model, and we provide the traction to accelerate your results.

A seamless clinical continuum

We remove the boundaries between trial phases. Our methodology connects early regulatory strategy, clinical execution, and real-world evidence into a single, cohesive workflow. Every step is designed with the next one in mind, ensuring critical clinical insights are never lost in transitions.

Combining global reach with mid-size agility, we deliver the scientific rigor of a global CRO without the bureaucratic lag. Your trial is never just another ticket: our dedicated teams immerse themselves in your science to anticipate risks and accelerate time to market.

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One team, whether you need a single specialist or a full trial.

Clinical development

Access specialized clinical experts who integrate directly into your internal teams, matching your operational demands as they shift.

— Rapid deployment of validated clinical professionals.

— Flexible capacity management  tailored to pipeline shifts.

Phase I to III Phase IV & RWE

Strategic solutions

We embed life sciences expertise wherever your programme needs it: a single expert consultant, a dedicated FSP team, a hybrid model or a fully managed function. Every option draws on 60,000+ active professional profiles and runs on one continuum, with built-in flexibility, trial security and senior teams that stay from day zero.

— Expert consultants matched to your study, on average within five days.

— Dedicated FSP teams, line-managed by TFS and working to your SOPs.

— Hybrid models that combine FSP and full service under one governance.

— Managed functions we run for you, from oversight to systems.

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End-to-end delivery

Full-service trial execution, backed by therapeutic depth and teams that stay.

— Full-lifecycle protocol management  from design to database lock.

— Scientific leadership across 5 specialized  therapeutic areas.

— Stable project teams ensuring continuous  data quality and safety.

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Quality Management

Three services. One independent quality function, standalone or embedded across your clinical portfolio.

— Audit & programme management: risk-based GxP audits to detect risks early and drive continuous improvement.

— Inspection readiness: targeted assessments, mock inspections and SME preparation for regulatory scrutiny.

— Quality oversight: ICH E6(R3)- and ICH E8(R1)-aligned oversight across studies and vendors.

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Global presence designed for local agility

International scale, deep local roots

We have built our structure by integrating established clinical teams across key markets, rather than handing off trials to unknown third parties. Operating directly on the ground allows us to navigate local regulations, streamline ethics approvals and keep recruitment on track.

Australia France Hungary Italy Norway Portugal Sweden United Kingdom Belgium Czech Republic Finland Germany Israel Netherlands Poland Spain Switzerland United States Canada Denmark

Clinical operations & outsourcing FAQs.

What clinical outsourcing models does TFS provide?

We deliver three modular frameworks under a single contract: Strategic Resourcing, Functional Service Provider (FSP), and Full-Service Trials. This model elasticity allows you to scale clinical capacity fluidly as your pipeline demands, eliminating vendor handoffs.

What is the geographic footprint and reach of TFS?

Founded in Lund, Sweden, we operate as a global CRO with active regulatory and clinical reach across 40 countries. We combine comprehensive multi-region execution with specialized infrastructure and investigator networks across Europe and the Nordics.

How does TFS maintain clinical study continuity?

We maintain an industry-leading CRA turnover rate of 14%, significantly outperforming the 20% sector average. This team stability ensures consistent protocol knowledge, reduces management burden, and protects your data integrity.

Which therapeutic areas does TFS specialize in?

We concentrate our medical, clinical, and regulatory capabilities exclusively within five core areas: Dermatology, Internal Medicine, Neuroscience, Oncology, and Ophthalmology, backed by a track record of 1,800+ completed trials.