At Techsol, our philosophy of customer success is directly a measure of the value we deliver through our products and services. We have been consistent in achieving our goals and winning our client's trust for the last 11+ years across our business engagements. Our partners have always admired our exceptional solution delivery through the synergistic value-generation pathways we have created in the pharma ecosystem.

What Sets Us Apart

Proven Scientific Solutions

As a full-range clinical research services provider, we have delivered scientific process solutions to several multi-national sponsor companies across different therapeutic areas using our highly experienced team of Scientists, Biostatisticians, and other Medical Professionals.

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Extensive GxP Technology Delivery Experience

Since 2010, we have been a trusted technology partner for several global sponsors. Having delivered over 170+ projects, we have a very strong technical acumen to solve business problems using the right technology.

Quality and Compliance Focus

We always strive towards delivering products and services with the highest quality by adhering to best practices, global standards and applicable regulations.

As an organization, we have ISO 9001:2015, ISO 27001, ISO 14155:2011 and ISO 13485:2016 certifications to account for GxP Quality and Compliance.

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Incremental Innovation Bandwidth

At Techsol, we have developed a culture that embraces a continuous growth mindset which is fostered by incremental innovation. The launch of SciMax Platform for Medical Affairs and the COMPIER platform for GxP Operations Oversight have led us to the forefront as emerging market leaders.

News & Updates

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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