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RIAR Consulting offers regulatory intelligence, compliance support, strategic decision-making, and market analysis for pharmaceutical and biotech industries.
At RIAR Consulting
We offer end-to-end support including pharmaceutical regulatory compliance, risk management, startup assistance, FDA & FSSAI liaison, gap analysis, and AI-powered decision-making across pharmaceuticals, food, and medical devices.
Providing expert regulatory guidance to ensure compliance across global pharmaceutical, medical device, and cosmetic markets.
Identifying, assessing, and mitigating regulatory risks to reduce approval delays and compliance failures.
Supporting manufacturers and distributors from regulatory planning to successful global market entry.
End-to-end regulatory support for medical devices and IVDs, including classification, documentation, and approvals.
Managing authority interactions with SFDA, US FDA, CDSCO, EMA, and MHRA through structured submissions and responses.
Ongoing regulatory support for renewals, variations, post-market compliance, and continuous regulatory updates.
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Whether you are a manufacturer, distributor, or healthcare innovator, RIAR Consulting delivers clear, reliable regulatory guidance across global markets. From regulatory intelligence to submission strategy and compliance execution, we help you make informed decisions, reduce approval risks, and achieve efficient market entry.
Stay aligned with current global regulatory requirements, guidance documents, and authority expectations across multiple markets.
Expert guidance on classification, documentation, submissions, approvals, and lifecycle compliance.
Understand regulatory trends, approval pathways, and competitive positioning within regulated life-science markets.
Tailored regulatory strategies designed for your products, markets, and business objectives—from planning to post-approval.
We Assess regulatory requirements and define the optimal approval strategy for pharmaceutical products. We Prepare compliant documentation and manage submissions across global regulatory authorities. We Support approvals, authority interactions, and ongoing regulatory lifecycle compliance.
To discuss your product, market, and regulatory objectives.
For an initial assessment and gap review.
Then initiate structured regulatory support.
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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