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

Enabling eSource in Clinical Studies to Optimize Trial Quality

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Implementing Electronic Consent for Clinical Trial Participation

Industry Background of eConsent In an attempt to address health authority concerns and improve patient confidence, companies and independent industry bodies have experimented with electronic consent (eConsent) using electronic media such as smartphones, laptops, and tablets. Despite positive outcomes, its implementation remained experimental until FDA officially released a guidance in December 2016. Following in FDA’s [...]

Top 4 Trial Design Best Practices for Medical Device Clinical Studies

What drives the growing complexity in medical device clinical trials? The medical devices industry has revolutionized medicine with significant advances in both detection and treatment of diseases. Clinical trials for medical device regulatory approval are designed to produce valid scientific evidence of safety and effectiveness for the intended uses. Moreover, sponsors must consider designing trials [...]

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