Techsol is specialized in providing fully-managed cloud solutions and professional consulting services for drug safety, signal management, PV operations management, compliance governance and advanced data analytics. With our domain expertise, we collaborate with clients to understand business challenges and resolve them with lean and congruent business solutions to scale-up quality, speed, operational efficiency and regulatory compliance.

Oracle Argus Safety & Empirica Signal

Safety System Strategic Consulting

Plan your long-term success by establishing and optimizing your Drug Safety Systems and Processes with our unparalleled subject matter expertise.

Oracle Argus E-Gateway and Empirica Setup

Leverage our expertise for the implementation of a Regulatory Compliant Drug Safety Platform using the GAMP-5 Risk-based validation approach.

Oracle Argus E-Gateway and Empirica Support

Establish an uninterrupted business process with our SLA-based specialized Argus, Insight and Empirica Signal application support.

Oracle Argus E-Gateway and Empirica Upgrade

With our Argus Service Desk, plan and execute all application upgrades and system configuration changes with risk-based Change Management.

Oracle Argus E-Gateway and Empirica Training

We offer hands-on end user and application administration training for Oracle Argus, Insight, E-Gateway and Empirica Signal.

Safety Case Data Migration

Use our validated accelerators to migrate from an on-premise data center to cloud or from another safety system to Oracle Argus.

Techsol's Compier Platform offers a wide-range of automation and insights driven modules for PV Operations Management, Quality and Compliance Oversight.

Compier Pharmacovigilance Modules

Latest Insights

Aggregate Reporting – Significance, Classification and Challenges

Aggregate reports are the cumulative reports in the database that emphasise on evaluation of safety profile and risk-benefit analysis of a drug. Aggregate reporting is the process of compilation and submission of aggregate reports to the regulatory agencies over the period of the product’s life cycle (during pre-marketing and post-marketing phase) to provide a comprehensive [...]

Literature Screening – Process overview, challenges en-route and the scope for automation

Medical and scientific literature is a valuable source of safety information that helps in monitoring benefit-risk profiles and emerging safety issues of medicinal products. Literature screening is conducted to ascertain abstracts and articles that provide crucial information on serious and non-serious Individual Case Safety Reports (ICSR) reports and risk-benefit assessment of a drug. The scientific […]

Oracle Argus Safety Application Upgrade

Key Highlights of the Latest Oracle Argus v8.2.3 Release and Why Its Important for Drug Safety Processes by Sriram Varma on May 10, 2021 In April 2021, Oracle released the new version 8.2.3 that addresses new regulatory compliance requirements, several functional enhancements, enhanced user experience and critical technology updates for the Argus Safety and Argus [...]

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