Clinical trials are the foundation of medical innovation, and they guarantee that new medicines, biologics, and medical devices pass rigorous safety, efficacy, and ethical tests before they are available to the public. This comprehensive guide delves into FDA and ICH regulations, including trial phases, GCP compliance, regulatory issues, and innovative trends such as Decentralized Trials (DCTs), AI-based research, and Personalized Medicine. Be at the forefront of the rapidly changing world of clinical trials and learn how groundbreaking innovations are redefining the future of drug and device innovation.
A must-read for researchers, sponsors, and industry professionals!