You are on a mission to discover, develop and deliver life-changing treatments and therapies that can save lives and sustain good health. To become successful in this endeavor, you need the right choice of technology that is powerful, regulatory compliant and reliable to manage scientific business processes and associated information. At Techsol, it is our passion to develop such cutting-edge technology that empowers your commitment to deliver that healthcare promise.

SciMax Global - Maximizing Value for Scientific and Medical Affairs

Techsol's subsidiary company, SciMax Global, exclusively focuses on delivering the industry's most advanced Medical Affairs platform to pharma and medical device companies. As a purpose-built system, it has a wide-range of technology capabilities for Medical Information, Scientific Publications Management, EAP & Grants portals, HCP and Patient Collaboration Portals, IIT / IST portals and other customer engagement modules to optimize various medical affairs functions.

Medical Technology

Working towards the digital transformation of Medical Affairs in your organization?

We can present a personalized platform tour that is aligned towards your business goals

COMPIER - Compliance, Competence & Collaboration Enabler

Compier is a process orchestration and compliance governance solution to streamline, track and report the outcomes of GxP operations and related cross-functional activities managed by sponsors across different vendors, partners and affiliates. The platform is engineered with modern technology to facilitate automation-driven process workflows and enables companies to take informed decisions using actionable insights.

Analysis Overview

Explore the Power of Automation and Data-driven Ops Oversight to Optimize Quality, Compliance and Productivity.

Eliminate Manual Trackers, Reduce Resource Costs and Maximize Opportunities for Operational Excellence

New Insights

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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