Our expertise, on your terms

Customizable Functional Service Provider (FSP) support that grows with your clinical trial.

Siron Clinical Customizable Functional Service Provider (FSP): Agility that puts you in control

At Siron Clinical, we know that clinical trials aren’t always predictable. With our Customizable FSP model, we provide specialist expertise and fulfill specific tasks and functions you need at every stage of your clinical trial. The service is flexible and adapts to your needs – we change with you. And because our experts integrate into your team and infrastructure, you retain control.

Why choose Siron Clinical?

You manage the service, we manage the people

The Customizable FSP contract you have with Siron Clinical is a service contract, not an employment contract, so we deal with all personnel side of things, saving you time and resources.

You get what you need, not what is best for us

The expert support we deliver is based on your need, rather than what we have as capacity

The specialist expertise you need

Our CRAs and project managers have extensive experience and knowledge across a range of therapeutic areas and trial types.

Retain overall control and oversight of the clinical trial

Our experts integrate into your strategy, decision-making, and project management.

Flexible Hybrid FSP model

Your contract can grow with your organization, which means Siron Clinical can operate as a full service CRO whenever you’re ready, allowing you to keep the same people, with the same expertise, throughout your journey.

Lower cost, more flexibility

As a small but global CRO, we can better adapt to your needs than larger organizations, so you won’t end up paying for services you don’t need.

FSP Features

Start-up with feasibility and CTAs

Patient recruitment and retention

Regulatory submissions

Investigator meetings

Project training

Clinical monitoring

Stastics and data management (with a partner)

eTMF solutions

Pandemic or crisis impact management

Risk-based monitoring

Project management

Audit and inspection preps

Consultancy

IWRS (with a partner)

Our Process

We’ll follow your lead.

With our Customizable FSP model, you decide what support you need and when, and you pay for what you get, helping you forecast and manage your budget.

Our process includes these steps:

Together, we determine the scope of the support you need

We define the tasks involved and approaches to get them done

We outline and agree on the details in a contract

 

 

When you’re ready, we scale to the next level together

 

 

Our Services

Customizable FSP

Our Expertise, On Your Terms

Customizable Functional Service Provider (FSP)

With our Customizable FSP model, we provide specialist expertise and fulfill specific tasks and functions you need at every stage of your clinical trial.

Project Management

A Seamless Extension of Your Organization

Project Management

Flexibility, innovation, and integrity guide our approach to project management and leadership for the success of your clinical trials.

Clinical Monitoring

Expert Support for Your Investigators and Teams

Clinical Monitoring

We povide passionate strategic knowledge, specific guidance, and expertise for study execution across multiple therapeutic areas.

Quality Assurance and Control

Accuracy and Integrity

Quality Assurance and Control

We pride ourselves on accuracy and integrity through a continual and dynamic process when it comes to quality assurance and quality control.

Regulatory Submissions

Globally Minded, Local at Heart

Regulatory Submissions

We take our role in regulatory submissions seriously, centrally managing the submission process carefully and efficiently.

Additional Services

Partnerships at the Core of Medicine

Additional Services

We are focused on sharing our expertise and building industry partnerships, for international and regional clinical research.
customized fsp services

How is Clinical Trial Success Defined in Europe?

Bringing a product further down the development pipeline often requires conducting clinical research in Europe. In the EU, the Clinical Trials Regulation harmonizes the submission process, but local requirements are still varied and specific to each country, and cultural differences can be challenging.

What defines clinical trial success in Europe? Download our RFI on to discover more about our insights, approach and experience.

Experience Matters

As an international contract research organization (CRO), we offer unparalleled knowledge, support, guidance, and experienced clinical research professionals to the biotechnology, life science, and medical device industries. We are committed to leading the development of new and advanced treatments by offering a range of CRO clinical trial services, from Customizable FSP to full-service.

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