Accommodating Last-Minute Design Changes
A prominent trial sponsor needed to accommodate eleventh-hour FDA requirements in the final days before First Patient In (FPI) for their pivotal global trial. During this tense time, the sponsor turned to the world’s leading Interactive Response Technologies provider for their expertise and newest generation IRT to ensure all changes were tested and ready in time for the study to go live on the expected date.
In this case study you’ll discover:
- Ways to avoid postponing the study start
- Tips for remaining in full compliance with FDA requirements
- Time-saving ideas to remain on track
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Utilize Almac Clinical Technologies’ expert team to ensure that your study objectives are fully understood and accurately implemented – submit an IRT request here for immediate review.
