Life Sciences

Regulatory Reporting Rules In Argus Safety

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In Argus Safety, all of the parameters for configuring the worldwide regulatory reporting rules are clearly identified on a single administration screen. You have the capability of selecting various case or event-level attributes, as well as using very advanced conditions, to focus the automated triggering of these report rules in various circumstances. 

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You also have the ability to name the report, select its destination, its form, as well as set all of the case/event attributes per report rule.

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Once the case is entered and assessed, the system can be configured to automatically schedule and generate the associated case-level regulatory reports scheduled by the configured rule.

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Be sure to check back soon, as we will cover periodic reporting in Argus Safety next. To read past posts in our Argus Safety features series, click here.

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Rodney Lemery

Dr. Rodney Lemery specializes in the implementation, support, and development of software used in the collection, management, and analysis of clinical data. His accomplishments as director of safety and pharmacovigilance at Perficient include the management of numerous clinical application implementation projects. In addition to his expertise in clinical and safety applications, Rodney is able to navigate between the technical and clinical worlds with ease due to his complementary educational background in epidemiology. He also holds a part-time professorship in the School of Health Sciences at Walden University, which solidifies his ability to lead global safety implementations at Perficient. Rodney has been with Perficient, via the acquisition of BioPharm Systems, since 2000. Prior to joining the company, he worked at Pfizer.

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