Forte’s development approach is to not only navigate industry regulations, but to strategize how to best serve and assist our community. Learn Forte’s philosophy towards developing 21 CFR Part 11 compliant systems.
Centralized monitoring can help monitors quickly identify problem protocols and/or sites to reduce regulatory risks, data errors and protocol deviations.
Don’t overlook these key factors when making your build vs. buy decision for a research evaluation and reporting system.
Use these five fundamental elements of clinical data management to implement quality data practices across your research organization.
Expert webinar presenters answer attendee questions about data quality best practices and steps to grow their careers in data management.
Join us for this free webinar to hear Shannon Labout of CDISC and Shannon Roznoski of Forte explore the value of quality data in clinical trials and the necessary skills for effective data management.
As a cancer center, tracking and fulfilling requirements to earn and maintain NCI-Designation can be complex, decentralized and resource-intensive. The task is especially difficult without standard procedures to collect data for the necessary reports. The Case Comprehensive Cancer Center needed a system to manage this process.
Creating processes that result in accurate, timely and complete data are invaluable when implementing or optimizing a CTMS. Here are a few tips to achieve your goals.
Learn how centralized data can help institutions efficiently and accurately report their research performance and discover the tools to help.