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Pharmaceutical & Biotechnology Compliance

Optimize resources, recalibrate business operations, and drive innovation for a healthier today and tomorrow.

Pharmaceutical business operations are continuously evolving with the dynamic pressures of market sustenance, changing regulatory compliance requirements, technology advancements, and improving bottom-line growth. These dynamic changes reinforce the importance of driving agility, innovation, and improving compliance in clinical and regulatory processes to realize better business outcomes by reducing time to market and improving patient experience. Tata Elxsi enables global businesses to unlock and create value in their R&D operations through its deep functional expertise, scalable global delivery capability, and digital technology-backed solutions.

Products & Services

Safety & Pharmacovigilance | Regulatory Compliance | Medical & Scientific Writing | Packaging & Labeling | Global Regulatory Intelligence

Safety & Pharmacovigilance

Tata Elxsi helps pharma & life sciences businesses in consolidating and standardizing internal processes and automating labor-intensive high volume tasks to streamline safety documentation for proactive action, operational efficiency, and enhanced market confidence in the brand.

Pharma Regulatory Compliance

Tata Elxsi helps companies in striking a balance between complex pharma regulatory documentation requirements through its homegrown global regulatory intelligence platform and cost-effectiveness amidst the dynamic and evolving regulations through optimization across the regulatory value chain.

Medical and Scientific Writing

Tata Elxsi provides a wide range of medical and scientific writing service offerings to pharmaceutical and biotech companies worldwide. We develop customized and marketable content for different communication channels to clearly and effectively communicate medical information to diverse stakeholders.

 

Pharma Packaging & Labeling

Tata Elxsi's pharma labeling services help manufacturers centralize, streamline, and automate label development processes to maintain label accuracy and integrity across the supply chain, while its packaging services help in designing sustainable packaging to ensure patient safety, longer product shelf life, and brand authenticity.

The Road Ahead

The latest technologies, partnerships, and media updates

Insights & Experiences

Customizable Cloud-based Global Regulatory Intelligence Platform
Case Study

Customizable Cloud-based Global Regulatory Intelligence Platform

The New EU Clinical Trial Regulation: What to Expect
Blog

The New EU Clinical Trial Regulation: What to Expect

Reimagine Patient Centricity with Digital Patient Engagement Programs
Technical Whitepaper

Reimagine Patient Centricity with Digital Patient Engagement Programs

Automating Regulatory Intelligence for the $10 Trillion Global Healthcare Market
Business Whitepaper

Automating Regulatory Intelligence for the $10 Trillion Global Healthcare Market

Understanding Safety Data Exchange Agreements
Blog

Understanding Safety Data Exchange Agreements

Combination Products: FDA guidance on the Principles of Premarket  Pathways
Blog

Combination Products: FDA guidance on the Principles of Premarket Pathways

AI-enabled SaMD and Digital Therapeutic Solutions: Good Practices for Commercialization
Blog

AI-enabled SaMD and Digital Therapeutic Solutions: Good Practices for Commercialization

4 things to know about Emergency Use Authorization in US and EU
Blog

4 things to know about Emergency Use Authorization in US and EU

Harnessing Technology for Intelligent Pharma Compliance Management
Blog

Harnessing Technology for Intelligent Pharma Compliance Management

Pharmacovigilance in the Digital Era – Know Your Safety Reporting
Blog

Pharmacovigilance in the Digital Era – Know Your Safety Reporting

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