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July 26, 2025
Imagine Ananya, a graduate student in pharmaceutical sciences in Pune. It’s late evening, and she’s working on her thesis about new drug formulations. She needs to reference the latest WHO GMP guidelines for injectables—but after hours spent flipping between PDFs and online sources, she’s frustrated. Then she tries Vera.
She simply types, “Show me the WHO GMP requirements for injectable drug container
integrity.” Vera responds instantly—a concise answer, directly citing the correct clause,
referencing the most recent document, and even suggesting related ISO standards. Just like
that, Ananya resumes writing. What used to take her hours now takes mere seconds
AI in pharma helps students and researchers quickly access complex regulations, simplifying understanding. QA pros save days as AI compares compliance differences, cuts errors by up to 40%, and reduces submission turnaround by 60%. Startups use AI to flag protocol issues, saving time and budget while boosting confidence before regulatory filings. This transforms pharma compliance and operations.
AI-powered regulatory platforms in pharma track global guideline updates, analyze changes, and predict policy shifts with up to 90% accuracy. For startups, this insight offers strategic foresight beyond compliance. Vera bridges the domain-access gap, serving as a trusted companion that delivers speed, accuracy, and context across user experiences.
This ecosystem is aligned with growing AI adoption—today, over 90% of pharma companies
are investing in AI for discovery, development, compliance, and marketing. Clear benefits are
emerging: reduced cycle times, fewer errors, smarter decisions, and operational
resilience.
AI empowers learners by making regulatory knowledge fast and accessible, saves regulators time and costs while enhancing compliance, and helps disruptors replace expensive consultants to speed market entry. Together, they drive AI-powered pharma transformation. Vera is live, and RIAR promises to scale and lead the future of pharma AI
Riar Consulting supports pharmaceutical, medical device, cosmetic, and emerging healthcare companies with structured regulatory strategies, submission management, and market entry support across major global regulatory authorities.
Stay informed with RIAR Consulting as we share key regulatory updates, compliance insights, and global market access guidance.Your trusted partner for efficient approvals across SFDA, US FDA, EU, UK, and India.
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