Optimizing Clinical Trials From Onset

Optimizing Clinical Trials From Onset

Data driven research to pin-point patient recruitment

The more informed and better engineered clinical trials are, the more likely they will stay within budget and be on time. This is why we offer comprehensive feasibility studies as a component of full-service trials and also as a feasibility consulting offering. Our goal is to save you time and costs in the long run.

At Synteract, we draw on our knowledge base of vast clinical research experience, site and patient advocacy relationships, regulatory considerations, and industry catalysts to provide a level of insight that is not attainable using traditional feasibility assessments.

While for some, feasibility assessments are synonymous with querying investigators and facilitating questionnaires, you can expect a more expansive and critical view of the clinical research environment from our feasibility analysis.

Synteract feasibility study services are customized to meet your specific clinical trial needs and include:

  • Protocol review and design analysis
  • Standard-of-care analysis
  • Epidemiology data analysis
  • Site profile analysis
  • Site and patient motivation assessment
  • Competitive landscape analysis
  • Feasibility data analysis
  • Screening and enrollment rate analysis
  • Geographic optimization analysis

For help mitigating the risk and optimizing the success of your clinical trial, contact us today.

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By submitting your information to us through this webform, your business details will be added to our database. In accordance with our Privacy Notice, we may then contact you with marketing information about Synteract that might be of interest to you. We will never sell your details to third parties. You can unsubscribe from marketing communications at any time.

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