In today’s global research landscape, clear and consistent communication is more than a necessity — it’s a strategic advantage. It is particularly critical in clinical trials, where data must speak a universal language across teams, geographies, and regulatory frameworks.

The CRF (Case Report Form) and CDISC (Clinical Data Interchange Standards Consortium) standards serve as the universal language of clinical trials, ensuring consistency, clarity, and collaboration across the entire study lifecycle. By implementing these essential frameworks, organizations can optimize data collection, management, and submission — driving cost efficiency and accelerating medical advancements.

Join us for an insightful webinar where our experts explore how CRF/CDISC standards support the design, execution, and analysis of clinical trials.
 

Key Topics 

• Benefits of adopting data standards 

• Key challenges and how to navigate them 

• Latest developments in CRF/CDISC standards and what they mean for your trials 

Speakers 

• Walter Briggs, Principal Clinical Data Manager 

• Juan Benavides, Senior Clinical Data Manager