What is Good Clinical Practice (GCP)?
Good Clinical Practice (GCP) is an international ethical and scientific quality standard for the design, conduct, performance, and monitoring, auditing, recording, analyses and reporting of clinical trials.
By ensuring Good Clinical Practice (GCP), that means that the data and any medical results were reported; are credible and accurate, in addition to certifying that the rights, integrity, and confidentiality of the subjects of trials are secured and totally protected.
What is the importance of Good Clinical Practice Course (GCP)?
Good Clinical Practice Course (GCP) is considered the main and first success factor for clinical research professionals; an amazing starting point for anyone who’s interested to work in the clinical research field.
The rules and principles of Good Clinical Practice (GCP) are helping in reassuring the safety, integrity, and quality of clinical trials through labeling specific elements related to the design, conduct, and reporting of clinical trials. Good Clinical Practice Course (GCP) including the description of the different responsibilities for each member in the clinical trial, like: investigators, sponsors, monitors, and IRBs in the conduct of clinical trials.
Good Clinical Practice (GCP) Course’s main goal is to ensure that:
- The safety, the rights, and well-being of human subjects are completely protected.
- Clinical trials are managed in line with approved plans with rigor and integrity.
- Data derived from clinical trials are reliable.
What will you benefit from the GCP course in AHC?
By joining Good Clinical Practice Course (GCP) which is provided by Andalusia Healthcare Conferences (AHC), you will absolutely notice the difference in each tiny detail, from the professional organization, to the accurate explanation by bunch of great experts.
Good Clinical Practice Course (GCP) is including the following topics:
- How to list the key drivers which led to the setting up of International Council for Harmonization (ICH) for GCP.
- How to explain the key considerations to be made with regard to GCP during a clinical trial.
- How to describe the roles and responsibilities of a sponsor, an investigator, and the IRB/IEC.
- Explaining the Adverse Event reporting requirements for both the sponsor and the investigator.
- How to List the core requirements for securing the informed consent of study participants.
- How to describe the importance of protocol compliance and clear documentation in the clinical trial process.
- How to define the purpose of various documents and templates which members need to use in the clinical trial process.
Need to know further information about the Good Clinical Practice (GCP) Courses brought by Andalusia Healthcare Conferences (AHC)? Feel free to contact us now and get all the details.
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