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

Oracle Argus Safety Login | Techsol

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 | Techsol Life Sciences

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 12 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

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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