Techsol specializes in delivering innovative scientific solutions for clinical drug discovery and development using a powerful combination of modern technology and data-driven insights. As a ‘Tech-enabled Scientific Solutions Provider’ (TSPO), we relentlessly work towards optimizing ‘Science’ with ‘Technology’ through constant knowledge expansion, continuous innovation, and identifying value diversification opportunities.

With the mission of optimizing medical research, developing novel treatments, and facilitating patient-centric care delivery, we partner with sponsors to deliver maximum value with uncompromised quality across the pharmaceutical product lifecycle.

Techsol Corporation Scientific Solutions Company

How We Deliver Technology Driven Scientific Process Solutions & Data Services

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As a TSPO, we seek to partner with sponsor companies to accelerate the development of drugs and devices across various therapeutic areas using our scientific expertise, quality focused processes and proprietary technology innovation.

All our end-to-end clinical development, pharmacovigilance, and ancillary post-marketing scientific services are delivered using regulatory compliant GxP technology that enhances process quality, operational efficiency, and reduces time to completion. We primarily focus on delivering services in the following segments.

Why Biopharma and Medical Device Companies Prefer Us as their Extended Technology Partner

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For over 11 years, our team has successfully delivered over 170+ enterprise level Life sciences IT Projects across different verticals. We are a leading GxP Technology Solutions Provider because of our proven capabilities in strategic consulting, technology selection, system implementation, computer systems validation, system integration, reports and analytics and application support.

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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