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

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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