Leading Contract Research Organization for Human Efficacy and Safety Clinical Trials
A Full Service CRO
Global Clinicals Incorporated is a full service contract research organization (CRO) based in Los Angeles, California that specializes in human efficacy clinical trials for validating product claims.
We will perform as much or as little to accommodate you the study sponsor and your product needs. We follow IRB review for all of our research projects. Additionally, we can write, design, and develop the study protocol and informed consent, scientific and medical research, submit to the IRB for approval, set up all patient files and case report forms, create and gather all source documents, screen and qualify and recruit all study patients, MD exam and enrollment of patients, lab services and blood chemistries(as needed), patient compliance, study site visits, statistical analysis of study data, final report, publish in scientific journal (if available), paperless data compilation, study summary. Every project is customized and follows the study protocol and GCP (Good Clinical Practice).
Our Expertise – Celebrating 15 Years
Global Clinicals, Inc. has a team of experts who have been participating in Clinical Research with a combined of over 100+ years in scientific and medical research
Global Clinicals, Inc. has the ability to initiate a study quicker than any other Clinical Research Organization, we can start your study tomorrow
Global Clinicals, Inc. provides seamless operations of your clinical trials
Global Clinicals, Inc. is celebrating 15 years in business as a leading CRO
Global Clinicals Incorporated is a full service contract research organization (CRO) based in Los Angeles, California that specializes in human efficacy clinical trials as well as bioavailibity and bioequivalence studies.