Supporting A Regulatory Submission Proactively
With this case study, you’ll not only discover the benefits of a superior partnership approach, but an innovative Interactive Response Technology (IRT) as well. Learn how the implementation of both helped to ensure that no manual variances affected the integrity of the data submitted to regulators on two extremely large Phase III trials for a global pharmaceutical company.
- Time-saving identification of scenarios that could result in manual intervention
- Efficient auditing of the data base, thus providing more in-depth information for regulators
- Well-organized information provided to ensure a smooth regulatory review process
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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.