The Trial Data Exchange will build a two-sided network, allowing sites and sponsors can easily access and share standardized clinical research data, including critical regulatory documents.
Centralized monitoring can help monitors quickly identify problem protocols and/or sites to reduce regulatory risks, data errors and protocol deviations.
Learn how a Master Delegation of Authority can streamline the delegation process by standardizing tasks at the organization level.
Use these tips to streamline training workflows for protocol staff at your organization.
Stuart Cotter of Forte details what key issues a research institution can address by implementing an eRegulatory system.