eLearning Solutions

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Delivery of e-Learning Solutions

Our custom developed eLearning solutions and capabilities enable Life Sciences and global Pharmaceutical customers manage enterprise user adoption and change management of various regulated applications and the associated infrastructure without compromising on quality.

We offer several ready to be deployed eLearning packages for industry leading solutions and also offer custom development services as per customer specific requirement. All of our ready to be deployed packages can further customised and enhanced as per the customer needs.

Our Capability

Our e-Learning content is SCORM 1.2 (Shareable Content Object Reference Model) compliant and customers can access our e-Learning catalogue available on our cloud-based Learning Management System (LMS) or host content in their in-house LMS. Our LMS is validated and meets all regulatory requirements such as  21 CFR Part 11 requirements  including audits, audit trails, system validations, electronic signatures and documentation.

Our e-Learning offering standard features include:

  • Graphically rich content and activities, reinforced by clearly defined learning objectives
  • Graphical workflow of the process for each module along with learning objectives
  • Assessment & summaries of all key points
  • Concluding ‘learning check’ module, to test knowledge retention

Techsol provides ready to be deployed comprehensive framework for online training and learning management capabilities on various industry solutions across Clinical Development, Pharmacovigilance and Medical Affairs processes.

  • Oracle Argus Safety Suite
  • Oracle Empirica Suite
  • Clinical One Platform
  • Oracle OC RDC TMS Suite
  • Oracle Siebel CTMS
  • SciMax Medical Information/ Affairs Platform
  • Techsol Compier Platform
  • Veeva Vault Platform
  • Veeva/ SFDC CRM
  • Axway Gateway

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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