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Welcome to the GCP Refresh course! In the ever-evolving landscape of clinical research, staying updated is not just a mark of excellence but a legal imperative. This course is specifically tailored for clinical researchers who, having already been trained in Good Clinical Practice (GCP), understand the importance of continual learning. With regulations constantly evolving, especially in regions such as the EU and UK, it's crucial to stay abreast of best practices, GCP updates, and practical nuances associated with compliance. Over the duration of this course, we will delve into these updates and revisions, ensuring that you remain at the forefront of clinical research compliance and best practices. This GCP Refresh course helps to ensure you are equipped with the latest knowledge and insights to continue making impactful contributions to clinical research.
ICH GCP is applicable to clinical trials of drugs (medicinal products).  Different standards apply to drug non-interventional studies (ISPE GPP) and medical devices (ISO 14155:2020). 
Delegates need Basic knowledge of clinical research and previous training in ICH GCP before attending
Please email office@icr-global.org for enquiries

•       Revisit the background and history (context) of the ICH and the GCP guidelines.
•       Re-affirm the main principles and requirements of ICH GCP and understand how these relate to EU and UK clinical trials regulations.
•       Recognize the significance of informed consent and its process.
•       Grasp the pivotal role of the investigator’s brochure, trial protocol, and record-keeping in ensuring participant safety and upholding data credibility in GCP.
•        Receive practical insights on how to navigate the common challenges and pitfalls in GCP compliance.
•       Gain up-to-date knowledge on the evolving GCP guidelines.
•        Be able to navigate your research responsibilities with increased confidence and efficiency, knowing you're aligned with the most current standards.