This comprehensive course will provide in-depth knowledge of Good Clinical Practice (GCP) principles, ensuring thorough understanding and adherence to the ethical and scientific quality standards for designing, conducting, recording, and reporting trials involving human subjects. The course will cover fundamental topics like the history and importance of GCP, roles and responsibilities of clinical trial stakeholders, informed consent procedures, trial design, data management, and safety reporting. Attendees will also be introduced to regulatory guidelines, quality assurance processes, and the effective utilization of the latest tools and technologies in clinical trials. The course will equip attendees with the skills necessary to maintain the rights, safety, and well-being of trial subjects, ensure data integrity, and navigate the complex regulatory environment of clinical trials, thereby making a significant contribution to the conduct of high-quality, ethical clinical research.

 

 

 

Do not hesitate to contact our administrator in case of additional questions (rebecka.lovborn@medhouse.se)