The British Association of Research Quality Assurance (BARQA) took a similar approach by combining Good Clinical Practice (GCP) and GLP in 2003 . The GCLP standards were developed with the objective of providing a single, unified document that encompasses IND sponsor requirements to guide the conduct of laboratory testing for human clinical trials.The Good Clinical Practice Certification is designed to give the researcher a basic understanding of the regulations and requirements for research using investigational (not approved by FDA) drugs or devices. This Certification is valid for three years, and can be earned by successfully completing one of the following options in Learn@Work: Complete a CITI GCP […]
CCRPS CRA Certification and CRC Certification is accredited by The Accreditation Council for Clinical Research Education (ACCRE) in June 2019 Code: 463-03-005-GPC08. ACCRE accredits the professional program in Clinical Research leading to the Certificate of Clinical Research. Evaluation and accreditation of this program is in accord with
GLPs are a set of standards which define the framework for a non-clinical study and states how they should be performed, evaluated, reported etc. To place a product in any market, it is necessary for a company comply with the GxP regulations. To know more about GxP regulations and how they can impact your business, reach out to us at sales
GCP Clinical Research is an ethical and scientific marker for conducting Clinical Trials. Compliance with the GCP (Good Clinical Practice) guidelines ensures that the rights, safety, and well-being of participants are valued and protected. GCP has an integral role in the success of Clinical Research and forms the foundation of Clinical Trials.
