Faster time to approval
Optimized revenue opportunities
Increased efficiency and accuracy
Improved planning and tracking of regulatory activities
Faster, more accurate Health Authority communications
Global compliance with current and future needs
Registration planning, tracking and management built for both your data and automation of your key processes.
A single regulatory database that will help you to avoid redundant data that exists within your submissions.
Trial master file misfiles are a common occurrence, with as many as one in every 10 documents being misfiled. In some ways, misfiles are an even greater issue now with eTMF systems, where filing is
Introduction Well, first and foremost, welcome! Rob Jones has relinquished control and I’ve been given free rein to bring you the last blog in the series on TMF Management in Clinical Trials. Those
Good morning, good afternoon, good evening (I like to cover every possibility because who knows when you are reading this)! I hope you all enjoyed part one of this series where we talked about the
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