MedSource
Clinical Research LLP
“Connecting Patients, Ensuring Safety, Delivering Quality Data”
About Med Source Clinical Research
At MedSource, we embark on a journey to redefine the future of healthcare through cutting-edge clinical research. As a leading Site Management Organization (SMO), we are dedicated to pushing the boundaries of innovation, accelerating the pace of clinical trials, and fostering collaborations that shape the landscape of medicine.
MedSource Clinical Research is a specialized Site Management Organization (SMO) that excels in the recruitment of patients and sites for clinical trials. Our unwavering commitment is to support pharmaceutical companies and Contract Research Organizations (CROs) in their vital mission to harness the significant patient recruitment potential and take advantage of cost-saving opportunities in emerging markets, with a primary emphasis on Asia.
While traditional study countries in Europe and North America have become expensive and potentially saturated with clinical trials vying for the same patient population, regions like Asia still present untapped and attractive potential. The strategic shift “Eastward” has proven highly effective for pharmaceutical companies, enabling them to streamline operations and focus on their core activities.
Yet, navigating the local infrastructure and understanding the cultural nuances of emerging regions can pose substantial challenges, making the difference between success and failure. At MedSource Clinical Research, we are well-acquainted with these obstacles and employ proven solutions to ensure accelerated patient recruitment while upholding the highest standards of data quality.
Our Services
Site Identification & Feasibility
Identification and selection of the optimum sites, Key Investigators and Opinion Leaders are fundamental to the success of any clinical trial.
Specialized Site Support
Rapid Start-up Accelerated Patient Recruitment & Enhanced Retention Overall Study Management
Regulatory Applications
We appreciates the significance of high quality submissions to the relevant Regulatory Authorities and Ethics Committees to ensure that approvals are available in a timely fashion
Training and Internship
We offers customized training programs to companies, professionals, investigators, sites and students in the field of clinical research.