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

How to Proactively Prevent Clinical Trial Protocol Deviations and Protocol Violations

Understanding the Importance of a Clinical Trial Protocol The fundamental objective of a clinical trial protocol is to provide common scientific guidance on how to conduct the clinical study in a regulatory-compliant manner and gather data that will ultimately provide answers on the safety and efficacy of the investigational medicinal product. The Guidelines for Good [...]

Food & Nutraceuticals: How Companies can Prove Health Value with Clinical Trials

What are Food and Nutraceuticals? ‘Nutraceuticals’ is a composite term of ‘nutrition’ and ‘pharmaceutical’. They are a blend of products that possess both nutritional as well as medicinal value. They are designed to improve physical health, boost immunity, and deal with stress and increase longevity. Nutraceutical products play a significant role in maintaining normal physiological [...]

Best Practices for Signal Management in Pharmacovigilance

Pharmacovigilance involves the collection, detection, assessment, and monitoring of data on Adverse Drug Reactions (ADRs) which must be evaluated to derive vital safety information. Signal detection involves monitoring the adverse reaction data for patterns that suggest new safety information. Safety signals can be detected from an extensive range of sources, such as spontaneous reports, clinical [...]

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