REGDEV INSIGHTS
Is Your TMF Inspection Ready?
In the complex world of clinical research, maintaining an inspection-ready Trial Master File (TMF) is crucial to ensuring the success of a study. A well-organized TMF not only allows for seamless audits but also helps identify and address issues before they
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Team Highlight: Brian Farnan
Sitting down with our GMP expert to chat about his passion for quality and compliance and what drew him to joining the RegDev
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How to Maximize Consultant Engagements
RegDev’s team of consultants are subject matter experts that partner with you to help you achieve your vision and goals. We want you to get the most out of your
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FDA Updates Guidance to Address Medical Misinformation
This revised guidance issued on July 8, 2024, replaces the 2014 draft guidance and is open for public comment for 60 days. Stay informed and help fight the spread of misinformation.
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RegDev Expands into Cybersecurity with New Team Member Rob MacPhee
Rob MacPhee joins the RegDev team as our new cybersecurity expert, bringing his deep knowledge and strategic insights to the life science
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