At their core AWS, Microsoft Azure and Google Cloud Platform offer largely similar basic capabilities around flexible compute, storage and networking. They all share the common elements of a The GCP - Social and Behavioral Research Best Practices for Clinical Research course introduces GCP principles and discusses how they apply to clinical trials using behavioral interventions and social science research. This course is presented in a dynamic, nine-module format with narration, interactive features, and downloadable resources. Good Clinical Practice Study Documentation. The Department of Medicine Clinical Research Unit has prepared this document is to provide guidance to all faculty and staff involved in the conduct of research on the best practices related to documentation. Good study documentation will allow for an individual with basic knowledge of the particular The ICH sets the standard that defines the guidelines for Good Clinical Practice (GCP). GCP is an international standard that ensures that ethical and scientific qualities are maintained in the designing, recording and reporting of clinical trials involving human subjects. ICH GCP in today's clinical research world is now more important 21 CFR 312 is a set of regulations issued by the US Food and Drug Administration (FDA) to establish good clinical practice (GCP) standards for conducting clinical trials. It covers the design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical investigations conducted under FDA regulations. The quality of data or goods resulting from scientific research must be held to high standards. For this reason, the GLP regulations, GCP guidelines, and GMP guidelines must be followed. Good Laboratory Practice (GLP) regulates the processes and conditions under which clinical and non-clinical research is conducted. .

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