The 2019 PRIM&R AER Conference provided insights into the changing regulatory world, and reaffirmed the importance of technology as processes and regulations continue to evolve.
Coordinating centers often struggle with the administrative burden of managing regulatory documents across multiple participating sites. We collaborated with our customers to address this challenge through the Forte eRegulatory Management System.
Integrated research systems can help streamline your operations, centralize workflows and reduce effort across your teams. But choosing your technology providers can have a big impact on long-term success at your organization.
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.