| Greetings!
We invite you to join our upcoming workshop focused on the newly released ICH E6(R3) Good Clinical Practice (GCP) guidelines, which represent a significant evolution in the design, conduct, and oversight of clinical trials.
This session will explore the latest regulatory expectations, including modernized trial methodologies, the integration of digital tools, and patient-centric approaches such as decentralized trials and telemedicine. Through real-world case studies and expert-led discussions, attendees will gain practical strategies for aligning operations with updated GCP standards.
This workshop is highly relevant for professionals involved in clinical trial design, monitoring, data management, and regulatory compliance who are seeking to stay ahead of evolving industry standards.
Register now to secure your place and learn how to confidently implement the ICH E6(R3) updates into your clinical research practice. | 
No comments:
Post a Comment