Resources
Compliance and Regulatory
How Your Approach to Regulatory Management Can Affect Disaster Recovery Readiness
Whether using paper, shared drive or vendor-provided systems to manage regulatory documents, research organizations need to ensure their data is safe in the event of a natural disaster.
[Q&A] Understanding, Achieving and Maintaining 21 CFR Part 11 Compliance
Expert webinar presenters answer attendee questions about 21 CFR Part 11 compliance and the validation process for electronic systems.
Understanding, Achieving and Maintaining 21 CFR Part 11 Compliance
Watch this webinar to hear our expert presenters provide an overview of 21 CFR Part 11 and discuss the roles both organizations and vendors play during the validation process.
Forte’s Approach to Development: 21 CFR Part 11 Compliance
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.
Enhancing Compliance and Identifying Risk through Centralized Monitoring
Centralized monitoring can help monitors quickly identify problem protocols and/or sites to reduce regulatory risks, data errors and protocol deviations.
Steps to Operationalize Your Coverage Analysis and Achieve Compliant Billing Outcomes
During this webinar, you’ll learn steps for operationalizing your coverage analysis across critical points of communication to achieve the billing, correct claims, and full reimbursement goals it drives.
Reduce Your Study Activation Timeline by Implementing Master Delegation of Authority
Learn how a Master Delegation of Authority can streamline the delegation process by standardizing tasks at the organization level.
3 Steps You Can Take Today to Accelerate Your Clinical Research Career
Take advantage of these three valuable opportunities to grow your career in clinical research and gain the necessary tools to make meaningful improvements at your current institution.