Biotech

The operational engine your biotech needs

You focus on the science of your project; we handle bringing it to patients. We organize the trial with investigators, manage your regulatory submissions and run daily operations on the ground. We start with the exact support you need today and scale at your pace, so you deliver the data your investors expect.

Talk to a therapeutic lead

Overcoming the barriers that stall your clinical development.

Consult with an expert

Your trial is never a low-priority account.

Bypass macro-CRO bureaucracy and rotating junior staff. Partner directly with senior scientists who communicate fast and take full ownership of your asset.

Protecting your timelines and funding runway.

Logistical delays burn your remaining capital before you reach key investor milestones. We secure field execution to deliver the clean data your board expects.

Honest guidance on the exact model you need.

Designing your first trial without prior ops experience can feel overwhelming. We guide you transparently to deploy only the clinical capacity required today.

How we secure your clinical pathway

Clinical continuum

Built-in flexibility, from a single CRA to full global trials.

Strategic resourcing, FSP and full-service clinical development, working as one team. Scale capacity across 40 countries, eliminating vendor handoffs while preserving protocol knowledge in the room the whole way through.

Therapeutic depth

Fast decisions through specialized clinical depth.

We restrict our focus to five complex therapeutic areas. Our specialized leads theyhold direct decision-making authority, fast-tracking approvals and solving site bottlenecks with scientific authority.

Teams that stay

True peers, driven by scientific urgency.

TFS holds an 88% retention rate, 8 points above the industry average. That means the senior scientific peer who joins your study is still there at database lock.

Trial security

Risk flagged early. Execution made visible.

Rooted in our Swedish heritage, we bring disciplined methodology and transparent communication to every study. We deliver real-time data integrity, flag protocol issues before they cost you time, and maintain regulatory compliance at every milestone.

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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Securing the path for sponsors’ science.

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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?

TFS holds an 88% retention rate, 8 points above the industry average. This team stability means consistent protocol knowledge, less management burden for your team, and stronger protection for 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.