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)
Project Management
A Seamless Extension of Your Organization
Project Management
Clinical Monitoring
Expert Support for Your Investigators and Teams
Clinical Monitoring
Quality Assurance and Control
Accuracy and Integrity
Quality Assurance and Control
Regulatory Submissions
Globally Minded, Local at Heart
Regulatory Submissions
Additional Services
Partnerships at the Core of Medicine
Additional 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.