Resources

Compliance and Regulatory

Latest Compliance and Regulatory Resources

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.

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[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.

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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.

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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.

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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.

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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.

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Research on Payments to Research Participants

Should clinical trial participants be compensated for their participant on a study? Take a look at published research on the compensation of research participants.

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FDA Specifies Patient Reimbursements vs Compensation to Encourage Recruitment and Equity in Clinical Trials

The FDA recently clarified its stance on participant reimbursements in clinical trials. What does that mean for the industry and your organization?

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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.

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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.

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