Home 9 Functional Service Provision (FSP)

Functional Service Provision (FSP)

 

So you have ultimate trial control.

That’s why.

Maintain Greater Control
Over Your Clinical Trials

The use of FSP models has become an increasingly popular trend in the biotech industry over the past few years. Many biotech companies seek to maintain greater control over their clinical trial operations while still leveraging the expertise and resources of CROs.

As a clinical CRO we can offer Functional Service Provision (FSP) in clinical trials by providing specific functional services to you on a project-by-project basis, utilizing specialized expertise and resources. This approach can help you to increase efficiency, reduce costs, and access specialized skills and knowledge on an as-needed basis.

Learn more about FSP in our blog.

What is Functional Service Provision? And how can you best make use of its benefits in your clinical research programs?

Selecting the right functional service provision partner is critical for the success of clinical trial outsourcing.

Clinical Trial Support
Throughout The
Product Lifecycle

The selection and implementation of functional service provision (FSP) models can vary between biotech and big pharma companies.  And, the specific functions included in an FSP model will always vary depending on your needs. However, some of the common functions included in our FSP portfolio are:

  • Clinical trial management
  • Data management
  • Biostatistics
  • Medical writing
  • Regulatory affairs
  • Clinical monitoring

  • Safety monitoring

  • Quality assurance and control

  • Project management

  • Site management and support

Clinical Research Insights

Case Study: Specialised Rescue Studies in Georgia

Case Study: Specialised Rescue Studies in Georgia

Discover how we successfully supported late‑phase clinical trials in Georgia by overcoming operational constraints, accelerating study start‑up, and restoring delivery confidence in complex research environments. This case study highlights three real‑world success...

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Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information

Big Enough To Cover All Your Needs.
Small Enough To Care.

Discover how Biomapas provides all the support to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Reliable support for every phase of your clinical trial, from recruitment to results.

Pharmacovigilance

Flexible safety monitoring to keep your products compliant and trusted.

Regulatory Affairs

Confidently navigate regulatory challenges with expert support.

Medical Information

Clear, accurate medical information 24/7, tailored for global audiences.

Quality Assurance

Export auditors help identify gaps and close them with actionable solutions.