About Site Identification & Feasibility

Often overlooked, choosing the right site is fundamental to generating the highest quality data and outcomes for your study. Accelagen has a strong database of site investigators, who we have worked with over a long period of time, to identify and determine the feasibility of various sites to execute your project. Our process for site selection involves matching the needs of your particular study and presenting a range of site preferences that align with the experience of the Investigator and other key resources and personnel. Once a site is nominated, we provide an assessment report of site qualities that also includes recruitment capacity and speed of enrolment, so that your clinical trial is as cost-effective and successful as possible.

In more detail

Risk

Aligning Investigators with your needs

Assessing which of our extensive network of experienced Investigators is best suited to your goals

Access to targeted patient population

Determining access and recruitment capacity so that your study can be completed as efficiently as possible

Comprehensive list of site preferences

Aligning your preferences with requirements for the Ethics Committee review process

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Assessing availability and readiness

Ensuring the availability of qualified site personnel and relevant equipment/facilities required to conduct the trial

Identifying gaps and barriers to success

From ensuring the Investigator/site has experience conducting similar trials, we look for confounding factors that may impact patient recruitment

Insurance and study procedures

Taking an holistic view of study procedures on Standard of Care as well as any relevant insurance requirements and payment procedures

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