InClin is pleased to announce that Good Clinical Practice, A Question and Answer Reference Guide – May 2017, Section 1, “GCP Regulations, Standards, and Guidelines for Clinical Research,” was reviewed and edited by Tony Cruz, DVM, InClin’s Vice President of Quality Assurance. This industry-leading GCP Question and Answer reference guide published by Barnett International is a key resource regarding the interpretation and implementation of US and international GCP standards for drugs, biologics and medical device clinical trials. The publication includes peer-reviewed, current and up-to-date overview of questions and answers regarding regulations, regulatory compliance guidance, and other topics to provide global regulatory compliance awareness with good clinical practice standards internationally.
“To be included on the board of editors of Good Clinical Practice exemplifies InClin’s position as a thought leader and expert on the latest regulatory guidance, regulations, comments, and developments for both drugs and devices,” said Dr. Cruz. “It is an honor to be among the distinguished international GCP experts involved in this publication”
A copy of the publication is available at http://www.barnettinternational.com/Publications/Good-Clinical-Practice–A-Question—Answer-Reference-Guide-2017/.
About InClin
InClin is a full-service Contract Research Organization (CRO) with offices in the San Francisco Bay Area and Sydney, Australia. We are a single source provider of an integrated full suite of clinical development services from Phase 1 through Phase 4, including project management, clinical monitoring, site and contract management, vendor management, data management, biostatistics, programming, drug safety, medical monitoring, medical writing, QA inspection readiness, as well as strategic consulting services. For more information feel free visit our website or contact us at our email address below.