Prospective Research Services (PRS)
Phone: +56 2 2897 9204
E-mail: info@prs.cl
Web: https://www.prs.cl/
PRS is a Contract Research Organization (CRO) headquartered in Chile and founded in 2014. We specialize in providing a diverse array of services to facilitate the initiation and advancement of clinical trials. What sets our services apart is our commitment to tailoring them to meet the unique requirements of each client. We employ a flexible work methodology that ensures efficient management of investigations.
Our delivery adheres to the highest international standards of Good Clinical Practices (GCP) and the International Council for Harmonisation (ICH), with a steadfast focus on acquiring robust and reliable data. At PRS, our mission is to facilitate clinical research excellence by providing our clients with comprehensive, innovative, and reliable services.
Our Core Values are INTEGRITY, EXCELLENCE, and COLLABORATION. At PRS, we are committed to conducting clinical research with the highest quality standards, compliance, and client satisfaction, providing: • Rigorous adherence to regulatory requirements • Continuous focus on process improvement • Client-centric approach to project management.
SOME OF OUR CLINICAL RESEARCH SERVICES: Study Design - Study Feasibility - Site Selection: More than 200 sites and Investigators selected. Study Start-Up: More than 150 sites initiated. Study Visits: More than 500 visits have been performed, including Pre-Selection, Initiation, Monitoring, Co-Monitoring, and Close Out. Some Therapeutic Areas of experience include Oncology, Infection Systems, Hematology, Gastroenterology, Medical Devices, Contraception, Rare Diseases, Endocrinology, Neuroscience, etc.
REGULATORY EXPERTISE: - Import License Management, - Regulatory Approvals, - Clinical Trial Agreement Negotiation, - Legal Representation, - Serious Adverse Events, and Safety Reports to the Institute of Public Health of Chile (ISP), - Management of contracts with Chilean regulatory authority (ISP)-authorized warehouses to ensure safe storage of investigational products and clinical trial supplies.
DATA QUALITY IS OUR PRIORITY: At Prospective Research Services (PRS), we adhere to our own Standard Operating Procedures (SOPs) that allow us to maintain focus and ensure clinical trial data information quality. Some activities related to overseeing and improving clinical trial quality assurance include: Co-Monitoring and Quality Visits. Audits Conducted and Support in Sponsor Audits. Regulatory Inspection Support.
KEY REASONS TO CHOOSE PRS • Expertise in navigating regulatory complexity • Timely and efficient execution of trials • Customizable solutions to meet unique needs • Commitment to quality, compliance, and client satisfaction Ready to partner with PRS for your next research endeavor? Contact us today to schedule a consultation and discover how we can support your clinical research needs. For further inquiries or to learn more about how PRS can support your clinical research goals, please contact us using the information provided.
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