Functional Service Provision (FSP)
So you have ultimate trial control.
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
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Clinical monitoring
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Safety monitoring
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Quality assurance and control
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Project management
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Site management and support
Clinical Research Insights
Unlocking Success: The FSP Advantage in Clinical Research
The Functional Service Provider (FSP) models in clinical research are becoming increasingly appealing to the pharmaceutical and biotechnology sectors, offering flexible and scalable solutions to outsource specific functions . Currently pharmaceutical and...
Bridging Gaps in Clinical Trials: Enhanced Access & Embracing Diversity
Explore the crucial role of diversity and accessibility in clinical research in this insightful article.
Contact Us
Contact us to learn about how we can enhance your clinical development, accelerate your path to Market Authorisation, and ensure compliance with local and global Post-Marketing requirements.
