Our Services

RIAR Consulting offers regulatory intelligence, compliance support, strategic decision-making, and market analysis for pharmaceutical and biotech industries.

Practice Areas

We Serve The Best Service

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.

Regulatory Support

Providing expert regulatory guidance to ensure compliance across global pharmaceutical, medical device, and cosmetic markets.

Regulatory Risk Management

Identifying, assessing, and mitigating regulatory risks to reduce approval delays and compliance failures.

Market Entry Support

Supporting manufacturers and distributors from regulatory planning to successful global market entry.

Medical Device & IVD Compliance

End-to-end regulatory support for medical devices and IVDs, including classification, documentation, and approvals.

Regulatory Authority Liaison

Managing authority interactions with SFDA, US FDA, CDSCO, EMA, and MHRA through structured submissions and responses.

Lifecycle Compliance Management

Ongoing regulatory support for renewals, variations, post-market compliance, and continuous regulatory updates.

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💡 Powered by Regulatory Expertise, Driven by Compliance

Get Clear, Accurate Regulatory Guidance — Fast

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.

Regulatory Intelligence

Stay aligned with current global regulatory requirements, guidance documents, and authority expectations across multiple markets.

Regulatory Consulting Support

Expert guidance on classification, documentation, submissions, approvals, and lifecycle compliance.

Market & Competitive Insights

Understand regulatory trends, approval pathways, and competitive positioning within regulated life-science markets.

Custom Regulatory Solutions

Tailored regulatory strategies designed for your products, markets, and business objectives—from planning to post-approval.

Trusted By

How We Work

Assess Regulatory Strategy Prepare Compliant Submissions Manage Approvals Lifecycle

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.

  • Step 1 — Schedule an exploratory consultation

    To discuss your product, market, and regulatory objectives.

  • Step 2 — Share your regulatory requirements and documentation

    For an initial assessment and gap review.

  • Step 3 — We define the regulatory strategy and execution plan

    Then initiate structured regulatory support.

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