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
We have a team of experts who have been participating in Clinical Research with a combined experience of over 100+ years
We have been involved in hundreds of research projects for small and large, public and private companies.
We have the FASTEST start up times over any other CRO or University, for any clinical trial.
We provide the FASTEST IRB submissions and approvals.
We provide seamless operations of your clinical trials.
We provide very competitive pricing and perform all services in the USA.
GLOBAL CLINICALS, INC. is celebrating 15 YEARS in business as a leading CRO.
When it counts, WE are the CRO of CHOICE!!!
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.