Accelerate clinical trial timelines.

The path to delivering innovative and effective clinical treatments requires navigating thousands of nuanced agreements and negotiations. For top global Biotechs, Factor’s Integrated Law™ approach for clinical trial agreements is not only guiding them through it all, but accelerating the process from lab to approval to market.

See for yourself

Jump-start a better process

Achieve faster cycle velocity

Leverage high-impact tech

Achieve peak velocity.

With over 350 proven lawyers, consultants and technologists at our disposal, our expertise in Contracting Managed Services allows Biotechs to accelerate clinical trials. Factor seamlessly integrates with clients and their Clinical Research Partners, negotiating on their behalf the full suite of agreements in each stage of the development process:

DISCOVERY AND DEVELOPMENT

PRECLINICAL RESEARCH

CLINICAL RESEARCH

REGULATORY APPROVAL

Learn how Factor can help

HOW WE DO IT:

Assemble a specialist team

Factor integrates a cost-effective team of experts and contract negotiators with expertise in clinical research spanning 40+ countries.

Transform while doing

We provide immediate capacity lift while building a repeatable and scalable model for your organization.

Establish strong business procedures and processes

We ensure contracts are prepared, negotiated, finalized, and maintained with consistency.

Build actionable metrics and insights

We build a foundation for fast-cycle process optimization and transparency, enabling smoother end-to-end collaboration across the clinical lifecycle.

Define what good looks like

We help establish and maintain negotiation guidelines and, as a result, free up your legal team from excessive escalations.

Integrate seamlessly into your systems

We accelerate the negotiation process with advanced, fit-for-purpose technology.

Faster start, quicker cycles

We bring data-driven insights and position analytics from countless site negotiations—leading to faster starting points and shorter negotiation cycles.

THE RESULT:

Accelerated launch

Three months faster new site start-up time achieved (multi-year US Biotech client)

Reduced cycle times

50% reduction in cycle time per agreement (compared to internal legal or CRO only)

Technology enablement

Modernized contracting operations with expert advisory, design and implementation services

Accelerate clinical trial timelines.

The #1 cause of clinical research delays.

Achieve peak velocity.

Get Integrated.

Accelerate clinical trial timelines.

The #1 cause of clinical research delays.

Achieve peak velocity.

Get Integrated.

Achieve peak velocity.