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Gain Actionable Insights On Quality, Compliance and Productivity Across GxP Processes

With the increasing availability of data, Pharma and Life Sciences companies can harness the potential of a robust business intelligence platform to derive powerful insights on various factors.

Techsol specializes in helping pharma customers in analyzing scientific data, and create insightful reports & dashboards for informed decision-making and operational excellence. Our experts help utilize technology to transform your information resources into actionable intelligence with its Business Intelligence and Analytics services. We have deep expertise with market leading, best-in-class enterprise analytics like OBIEE, Logi Analytics, BusinessObjects, Cognos, SiSense and other leading BI platforms.

How We Provide Answers To Your Business Questions Using Data

  • Understand your Business Goals and Gather Requirements for Different Types of Reports and Dashboards from Key Stakeholders
  • Complete Reporting Solution Design suitable for your enterprise with the required data sharing security controls
  • Develop, Test, Validate and Deploy interactive Reports and visual Dashboards tailored for Different Business Users

How We Help Clients

Analytics IconAccelerated BI/ Analytics domain frameworks that can help address business reporting requirements much faster by employing reusability and industry best practices.

settings iconReady to use data models, integration adapters and common data collection frameworks.

Reporting setting icon

Experience with most of the industry standard BI/Analytics platforms.

Computer setting iconCustom development of point to point adapters, frameworks, visualizations, reports etc.

Bi Reporting iconDomain specific BI expertise in Clinical Development, Laboratory Information, Drug Safety/ Signal Management, Medical Affairs/Information, Manufacturing Automation, Enterprise Quality and Commercial.

Analysis Overview

Types of Dashboards We have Developed for Clients

  • Strategic Decision Making and Ranking Dashboards
  • Operations and Performance Summary Dashboards
  • Process Productivity and Outcomes Dashboards
  • Quality, Risk and Compliance Dashboards

New Insights

Enabling eSource in Clinical Studies to Optimize Trial Quality

Source data is all information in original records and certified copies of original records of clinical findings, observations, or other activities in a clinical trial necessary for the reconstruction and evaluation of the trial. Electronic data source or eSource is the data that is initially recorded in electronic format in this process. Biopharma and MedTech [...]

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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