Looking for a leading contract research organization (CRO) that provides full service? Global Clinicals Inc. can help. Specializing in human efficacy and safety clinical research trials as well as bioavailability and bioequivalence studies.
We are committed to accommodating your needs, the study sponsor. We know how important research can be to the success of your products. Our company uses IRB review for all of our clinical research projects. Additionally, we write, design and develop the study protocol and informed consent, as well as various source documents. Providing scientific and medical research, IRB submission process, set up all patient files and case report forms. Our comprehensive process includes creating and gathering all source documents, screening, qualifying and recruiting study patients.
GCI manages all site operations, regulatory, MD exams, patient recruitment and randomization, lab services and blood chemistries(as needed), patient compliance, statistical analyses, etc . This process is efficient and effective. We have proactive marketing to acquire study candidates. We compile all data and analyze statistically, which is necessary for the final report. A study may be published in a scientific journal which is a welcomed goal, we can help. We provide paperless data compilation and a study summary. Every project is customized and follows the study protocol and GCP (Good Clinical Practice). We are ready to perform your study and expeditiously.