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Pharmaceutical & Biotechnology Compliance
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.
TEDREG - A Global Regulatory Intelligence Platform
An intelligent platform built to aggregate and organize the latest regulatory updates from major regulatory bodies across the globe and provide actionable insights to the manufacturers for new market launches and product sustenance in the existing markets.
The Road Ahead
The latest technologies, partnerships, and media updates
Insights & Experiences
Case Study
Customizable Cloud-based Global Regulatory Intelligence Platform
Blog
The New EU Clinical Trial Regulation: What to Expect
Technical Whitepaper
Reimagine Patient Centricity with Digital Patient Engagement Programs
Business Whitepaper
Automating Regulatory Intelligence for the $10 Trillion Global Healthcare Market
Blog
Understanding Safety Data Exchange Agreements
Blog
Combination Products: FDA guidance on the Principles of Premarket Pathways
Blog
AI-enabled SaMD and Digital Therapeutic Solutions: Good Practices for Commercialization
Blog
4 things to know about Emergency Use Authorization in US and EU
Blog
Harnessing Technology for Intelligent Pharma Compliance Management
Blog
Pharmacovigilance in the Digital Era – Know Your Safety Reporting
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