At MEDISCIS “Medical Science Services” our volunteer database gives us access to a large pool of study candidates.
With key information including medical and surgical history, current medical treatments, BMI, etc., as well as site preference and previous clinical trial participation, we are able to perform a 1st round query of inclusion/exclusion criteria based on your study Protocols and Informed Consent Forms
(ICF).
Following the 1st round identification, subjects are contacted via e-mail / SMS / telephone to propose participation. We also have additional communication outlets via internet, print media, journalism, and mailings. Potential study participants are scheduled for a screening appointment with the Medical Investigator to determine final study inclusion/exclusion. Once volunteer recruitment has begun, study status is closely managed to ensure that participation criteria and study timelines are met and maintained.
Recruitment Activities
