Author: Ann Ackley-Fifer

For nearly 30 years, the ICH GCP guideline has set the international standard of ethics and quality for conducting clinical trials.  The latest version, ICH GCP E6 (R3), was adopted on 06 Jan 25, an update 9 years in the making.  It contains an entire appendix dedicated to the Trial Master File.  Let’s explore some…

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advancement as a Veeva Premier Services Partner for Veeva Development Cloud.

Ensure a Smooth and Compliant Migration with Expert Insights Migrating to Veeva Vault Safety is a critical step for life sciences organizations seeking compliance, scalability, and efficiency in pharmacovigilance operations. However, data migration presents unique challenges, from source-to-target mapping to data integrity and regulatory compliance. What’s Inside the Guide? Key Benefits & Challenges of migrating to Veeva Vault Safety Technical Approaches &…