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

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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