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Legal AI Solutions for Pharmaceutical

Automate CDSCO drug approvals, clinical trial agreements, and patent management for pharma companies. Cut compliance time by 70%. 300+ firms trust Vidhaana.

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Vidhaana AI legal platform dashboard for Pharmaceutical compliance and contract management
70%
Faster CDSCO Review
300+
Pharma Firms Served
3x
Faster Clinical Trial Review
99.9%
Patent Deadline Accuracy

Powerful Features for Modern Legal Teams

Everything you need to transform your legal operations with AI

Drug Approval & CDSCO Compliance

Track CDSCO drug approval timelines, new drug application submissions, and regulatory circulars. AI alerts for schedule changes, import license renewals, and clinical trial approvals.

Clinical Trial Agreement Review

Review CTA, site agreements, and principal investigator contracts. AI identifies protocol deviations, indemnification gaps, and IP ownership clauses that create liability exposure.

Patent Portfolio Management

Monitor patent expiry, competitor filings, and FTO searches. AI tracks evergreening opportunities, compulsory licensing risks, and patent opposition proceedings at IPO India.

Pharma Regulatory Research

Search CDSCO guidelines, pharmacovigilance regulations, and Schedule M updates instantly. AI summarizes applicable rules for new drug categories across Indian and international markets.

Why Choose Vidhaana?

Join 9,600+ legal professionals who have transformed their operations with AI

Cut CDSCO compliance review time by 70%
Automate clinical trial agreement drafting and review
Monitor patent expiry and competitor filings in real time
Track Schedule M and pharmacovigilance deadlines automatically
Enterprise-grade security for proprietary drug formulations
Integrate with regulatory submissions and dossier management systems

Common Use Cases

Contract Review

Compliance Automation

Legal Research

Document Management

Trusted by Legal Teams Worldwide

See what our customers say about transforming their legal operations

"CDSCO approval tracking used to require a dedicated team. Vidhaana automated monitoring across all our product categories and saves us 20 hours per week."

Dr. Ramesh Pillai

Head of Regulatory Affairs, Pharmaceutical Company — Hyderabad

"Clinical trial agreements across 15 CROs now go through Vidhaana's review first. We catch indemnification gaps that previously required senior counsel involvement."

Anita Sharma

General Counsel, Biotech Firm — Pune

"Patent expiry monitoring for our 400+ molecule portfolio is now automated. We have not missed a renewal deadline since implementation."

Dr. Sanjay Krishnan

VP Legal & IP, Generic Pharma — Mumbai

Frequently Asked
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