Oracle Argus E-Gateway and Empirica Training

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Our Drug Safety System Training Services

With our Oracle certified SMEs (Argus Safety suite, Empirica Signal and Gateway applications), we can deliver training using the “Train-the-Trainer” approach to client appointed champions. Users are broadly classified as end users such as data processing, submissions, reporting and medical reviewers. Trainings can be delivered in several rounds over several hours as per the specific needs of the project.

Based on your business need, the following types of training can be delivered either with the classroom instructor-led model or by using the ‘Train-the-Trainer’ approach.

  • Configurations Management Sessions
  • Application Administrator training
  • End-user training for Case Management
  • Superuser training for System Administration

What Do We Offer

Our standard Argus Safety training includes following topics:

  • Case processing
  • Expedited reporting
  • Periodic reporting
  • P&L configuration
  • Workflow configuration
  • Admin Console configuration
  • Analytics
  • J lock
  • New features included in Argus J
Project Plan

Thought Leadership

How to Proactively Prevent Clinical Trial Protocol Deviations and Protocol Violations

Understanding the Importance of a Clinical Trial Protocol The fundamental objective of a clinical trial protocol is to provide common scientific guidance on how to conduct the clinical study in a regulatory-compliant manner and gather data that will ultimately provide answers on the safety and efficacy of the investigational medicinal product. The Guidelines for Good [...]

Food & Nutraceuticals: How Companies can Prove Health Value with Clinical Trials

What are Food and Nutraceuticals? ‘Nutraceuticals’ is a composite term of ‘nutrition’ and ‘pharmaceutical’. They are a blend of products that possess both nutritional as well as medicinal value. They are designed to improve physical health, boost immunity, and deal with stress and increase longevity. Nutraceutical products play a significant role in maintaining normal physiological [...]

Best Practices for Signal Management in Pharmacovigilance

Pharmacovigilance involves the collection, detection, assessment, and monitoring of data on Adverse Drug Reactions (ADRs) which must be evaluated to derive vital safety information. Signal detection involves monitoring the adverse reaction data for patterns that suggest new safety information. Safety signals can be detected from an extensive range of sources, such as spontaneous reports, clinical [...]

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