Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. Basic courses provide in-depth foundational training. We also offer completely fresh content in Refresher courses for retraining and advanced learners. GCP training supports clinical development of new medicines by: Educating staff in the fundamentals of ethical research. Ensuring that the work is done in accordance with standards. Ensuring that staff members know their roles and responsibilities. Ensuring the quality, accuracy, and credibility of the data. Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE). They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards The Good Clinical Practice (GCP) guideline is the international ethics and scientific quality standard for conducting clinical trials. In accordance with the National Clinical Trials Governance Framework, clinical trial investigators and their clinical teams must undertake training in GCP. More broadly, the Office for Research requires GCP of professionals entering the clinical trial research area. We highly recommend anyone, whether a novice in the clinical trials research area or experienced, wishing to learn more about the basic modern concepts of human research ethics and clinical trial research methodology to study this manual. The audience can equally be professionals What is GCP and why GCP is important in clinical research. The link between the Declaration of Helsinki and current GCP. The definition of the key definitions of terms and concepts used in clinical research, including stakeholders and key processes involved . The ICH-GCP Principles and practical advices to apply them in your clinical trials Good clinical practice is a guideline adopted internationally as standard operating procedure for conduct of clinical research. Despite these guidelines being available, unavailability of internationally harmonized framework for managing research fraud and misconduct makes clinical research a highly vulnerable area to commit fraud. • GCP is defined as a standard for the design, conduct, performance, monitoring, auditing, recording, analysis and reporting of clinical trials or studies • Good Clinical Practice is an international quality standard, which governments can then transpose into regulations for clinical trials involving human subjects. (Wikipedia) GCP enables different users to access the project thereby enabling easy collaboration. Google uses top notch security features and experts which make GCP one of the most secure platforms to use. The data stored on GCP is reliable as, if one datastore is unavailable the system immediately makes a secondary datastore available without any Good clinical practice (GCP) guidelines are an internationally recognized standard for clinical trials that include ethical and quality requirements that must be adhered to for any clinical trial that involves people. It specifies good clinical practice guidelines for all aspects of a study, from trial documentation and protocol amendments to xvrU.