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PRS Clinical, Ltd. is a full service Clinical Research Organization (CRO), offering clinical trial support in Phase I-IV studies, with operations in strategic countries on all continents. These countries are characterized by significant numbers of potential study subjects, often unmet medical needs, certain disease types that may not be as prevalent elsewhere, and highly qualified investigators. Data developed in local research centers have been shown to be of high quality and acceptable to the most demanding regulatory agencies worldwide.

 
Our main specialization is strong local presence in each of the markets, thorough understanding of local medical practices, customs, languages, as well as local research and regulatory requirements. We work through a network of pre-qualified, experienced investigators, which helps ensure strict GCP compliance, competent research activities, and high quality of data. Unlike some other CROs that often start looking for potential local monitoring support only when bidding on a multinational project, our existing global organization offers up-to-date regulatory consulting about local requirements, easily performs thorough feasibility studies, and allows rapid study start-up with subsequent good enrollment of patients.
 
We continue to expand our operations and are constantly adding new investigators to our growing network.