Navigating Regulatory Complexity: Understanding the Impact of ICH GCP R3 and Global Compliance in Clinical Trials
By EmVenio Clinical Research
Download this webinar to understand the implications of ICH Good Clinical Practice E6 (R3) – a pivotal shift in how clinical trials are designed, conducted, and overseen, with an emphasis on adaptability and innovation. Moderated by Deb Guattery, a seasoned quality expert at PCM Trials, the panel of regulatory, legal, and operational experts explore how the new update is reshaping the regulatory landscape in clinical trials and how sponsors and service providers can adapt proactively in order to build quality into every layer of their trial.