For over 11 years, Techsol has been a trusted technology partner with Oracle in delivering fully-managed and professional consulting services for various Oracle Health Sciences applications. With our hands-on experience and domain knowledge, we collaborate with Oracle to deliver best-in-class technology solutions and services to several global biopharmaceutical, medical devices and contract research organizations.

Our Practice Areas and Technology Expertise

Techsol Oracle Argus Safety

Oracle Argus Safety

With our certified team of Argus Safety Specialists, we provide the following technology solutions:

  • AccelSafety – A fully-managed Oracle Argus Safety Application Suite offering from Techsol for Biopharmaceutical and Device Companies
  • Rapid implementation of Oracle Argus Safety directly on Oracle Cloud
  • SLA-based Argus Service Desk for Application Support (Requests, Incidents & Change Management)
  • Argus DB Disaster Recovery and Business Continuity
  • Oracle Argus Safety Integrations
  • Custom Argus Safety Reports and Analytics

Oracle Clinical One

Clinical One

Our team of certified Clinical One specialists are readily available to deliver high-quality professional services to adopt, adapt and derive value throughout the clinical development lifecycle in this powerful platform. Listed below are the business services offered by Techsol by working with the Oracle Health Sciences Group.

  • Clinical One Systems Management Services (Implementation, Validation, Data Migrations, Training, UAT, etc.)
  • Functional Services (Clinical Operations, Biometrics, CDM, Medical Coding, etc.)
  • Value-added Custom Integration Solutions (eTMF, CTMS, Argus Safety, e-Adjudication, etc.)

Watch our Presentation with Oracle

Siebel CTMS

Oracle Siebel Clinical Trial Management System

AccelCTMS™ is a ready-to-use packaged, cloud-based, clinical trial management solution offered by Techsol using Oracle Siebel CTMS and Oracle Clinical Data Analytics Applications. Our solution enables holistic management of critical clinical trial activities from study start to site closeout for global clinical studies. Emerging biopharma, device manufactures, and contract research organizations can leverage AccelCTMS to plan, manage, and track early to late-stage clinical trials

Our Other Capabilities:

  • Rapid implementation of Oracle Siebel CTMS Cloud
  • Oracle Siebel CTMS Service Desk, Disaster Recovery and Business Continuity
  • System Integrations (EDC, eTMF, IWRS, Argus Safety, etc.)
  • Reports and Analytics (Study / Site / Subject Metrics, Trial Progress Summaries, Payments & Expenses, etc.)

For over 10 years, Techsol has been providing a robust EDC platform to emerging biopharma companies to centrally manage clinical trial data using Oracle Clinical, RDC and TMS applications. Over a dozen pharma and biotech companies have relied on Techsol’s eClinical platform for executing their Clinical Data Management operations.

New Insights

4 Effective Strategies to Accelerate Site Selection to Activation

Introduction to the site selection process Clinical research organizations (CRO) predominantly rely on the internal networks and investigator database to support a clinical study for a drug. As the clinical sphere continues to expand at a rapid pace, there is an upsurge in demand for clinical trial sites worldwide. CROs are striving for new sites […]

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 […]

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