The complexities involved in regulatory safety reporting necessitates proficiency to ensure quick access to intelligent data. The capture and analysis of safety data are critical in clinical trial management, as trials ultimately must demonstrate safety as well as efficacy.
PureSoftware provides Pharmacovigilance services that allow long-term success. Our consultants address the issues related to drug safety and process consistency, like the new compliance requirements, and can integrate safety data from dissimilar sources.
We provide professional services on the Argus product in the following areas:
AE Collection
and Follow-up
Case Entry
and Processing
Monitoring
and Analysis
Reports Generation and Customization
Proactive PV & E
PureSoftware understands that the quality and integrity of the data are of primary importance.
know moreClinical Data Management is a critical phase in clinical research, and data integrity is of paramount importance.
know moreThe complexities involved in regulatory safety reporting necessitates proficiency to ensure quick access to intelligent data.
know morePureSoftware offers a spectrum of integrating applications and infrastructure services tailored to meet client-specific needs.
know moreWe value partnering with life sciences organizations and develop technology-based solutions for them.
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We have some of the World’s Best Life Science Organizations relying on us.
You can become the next one.