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Functional Service Provider

GForce Life Sciences

Functional Service Provider

 

GForce Life Sciences’ Functional Service Provider (FSP) practice offers clients the flexibility that they need in managing clinical trials. Offering a variety of “a-la-carte” services, as opposed to a full suite of services, clients can outsource only what they need to fit their budget and/or other key components.

As strategic preferred provider partnerships turn out to be neither strategic nor preferred, many clients are pursuing FSP models for clinical research like GForce’s. We pride ourselves on our ability to collaborate, communicate, & listen well with all parties because communication is key to a successful project.

What We Can Do for You

 

When it comes to FSP outsourcing, we have an extensive array of services aimed at helping you navigate the clinical trial phase successfully. These include project and program management to cover practically everything related to the process. We also can provide you with site selection and management to take these elements off your shoulders.

 

During the testing, we can keep a close eye over every aspect with safety, medical and clinical monitoring. You also can count on our expertise to deliver expert data management, biostatistics and medical writing. If you have additional needs that you don’t see here, you can get in touch with us to find out more about our clinical trial FSP capabilities.

 

These FSP services are offered across all phases of clinical development & on medical device & IVD studies, lab studies, regulatory, and quality from study start-up through presentation and transfer of the final deliverable.

 

Why Outsourcing Makes Sense

 

Choosing us to be your functional service provider for clinical trials gives you numerous advantages. You maintain control over the project and your data, even as we execute all the services for you. With us working for you, you gain the resources you need quickly, without worrying about maintaining the same level of staffing once the trial is completed. There’s no need to add additional office space or invest in any other extra capacity. Not only does this save you a significant amount of money in terms of operational costs, but it also means you can concentrate on your core business processes without sacrificing any of your internal bandwidth.

 

When you turn to us to provide your organization with our FSP abilities, you also mitigate risk while gaining access to new markets and new opportunities. We make it easy to take those first steps into new territory without putting everything on the line. You also can be certain that you’ll be working with a partner who is dedicated to assessing your needs and developing a plan of action that is geared entirely around fulfilling them. To learn more about what we can do for you, get in touch with us today.

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  • Project and Program Management

  • Clinical Monitoring

  • Safety & Medical Monitoring

  • Site Selection & Site Management

  • Data Management

  • Biostatistics

  • Medical Writing

  • Subject Matter Expertise not addressed above

 

These services are offered across all phases of clinical development & on medical device & IVD studies, lab studies, regulatory, and quality from study start-up through presentation and transfer of the final deliverable.

  • Hire an FSP to execute the services, while still maintaining control of job & data

  • Focus on Core Business Processes

  • Lower Operational Costs

  • Improved Quality

  • Gain Resources

  • Mitigate Risk

  • New Market Access

  • Gain Services with Relevant Expertise

  • Decrease Need for Line Management

  • Reduce/Save Office Setup Costs

  • Retain Control of YOUR Data