Resource Library

Lessons from FDA 483s—Fortifying Clinical Trial Integrity

FDA Form 483s, issued after clinical trial inspections, expose recurring vulnerabilities that threaten data quality and regulatory trust. Analyzing recent …

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A Promising Step Towards Increasing Patient Diversity in Clinical Trials

With over 128,000 new cancer cases diagnosed annually, Nigeria presents a unique and incredibly diverse hub for facilitating drug development. …

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Elevating Standards: ClinFocus Announces ISO 9001:2015 Certification

ClinFocus is pleased to announce that it has achieved ISO 9001:2015 certification, an internationally recognized standard that ensures a quality …

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The Transformative Power of Collaborations and Partnerships in Clinical Research

In the dynamic realm of clinical research, a notable trend is reshaping the landscape—collaborations and partnerships. The traditional model of …

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The Rise of DCT Technology Solutions in Clinical Trials

The FDA defines decentralized clinical trials as “those executed through telemedicine and mobile/local healthcare providers, using processes and technologies that …

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ClinFocus Harnesses AI to Elevate Data Quality Efficiency in Clinical Data Management

ClinFocus, a prominent leader in Clinical Data Management and Biometrics services, is excited to announce a significant stride in its …

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