At ADAMAS, we don’t just interpret regulatory change—we help you lead through it.
The transition to ICH E6(R3) isn’t business as usual. With its emphasis on risk-based quality, patient-centricity, and data integrity, this revision marks a fundamental shift in how clinical trials are designed, managed, and monitored. For sponsors and service providers alike, adapting to these changes isn’t optional—it’s essential.
In this free guide, we break down the most critical updates to ICH E6(R3)—and provide practical, inspection-ready strategies to help you stay compliant, audit-ready, and ahead of regulatory expectations.
Download the guide to discover how ADAMAS helps organisations like yours:
- Navigate the complexities of E6(R3) with confidence
- Implement risk-based quality management systems
- Strengthen oversight of service providers and decentralized trials
- Optimize SOPs, training, and inspection readiness
- Leverage expert consulting to ensure a smooth, strategic transition
Get your copy of the guide and start planning your path to full ICH E6(R3) compliance—today.
