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ABOUT AAHVI PHARMA
Your Trusted Partner in Pharma Compliance & Licensing
AAHVI PHARMA PVT. LTD. is a Hyderabad-based pharmaceutical consultancy and distribution company, specializing in end-to-end regulatory, licensing, and compliance services for the pharmaceutical industry. From R&D site approvals, dossier preparation, and manufacturing licenses to import/export registration and product compliance, we serve as a strategic partner for pharmaceutical companies navigating India’s complex regulatory ecosystem. With hands-on experience across APIs, formulations, and clinical research segments, we align operations with the latest requirements under the Drugs & Cosmetics Act, NDCT Rules, and CDSCO/DCGI frameworks.
What sets us apart is our commitment to accuracy, efficiency, and accountability in every regulatory interaction. We don’t just assist with approvals — we drive outcomes. Whether you’re a startup entering the market or an established manufacturer scaling globally, AAHVI ensures your compliance journey is smooth, secure, and successful. Your compliance is our responsibility. Your success is our priority.
Our Vision
At Aahvi Pharma, we are guided by a commitment to ethical innovation, quality-driven manufacturing, and patient-centric care. We believe that access to safe, effective, and safe
Our Mission
To become a trusted global leader in pharmaceutical innovation and manufacturing, delivering high-quality, affordable medicines that enhance and extend human life across every c
Our Motto
To research, develop, and deliver high-quality pharmaceutical products that meet global standards, driven by innovation, ethical practices, and a deep commitment to improving patient health
Our Capabilities
We offer regulatory expertise that spans across product registration, compliance filings, government liaison, and pharma documentation for Indian and global markets.
- Preparation and filing of CT forms under NDCT Rules 2019
- Dossier preparation for R&D, DCGI, and CDSCO submissions
- Licensing support for manufacturing, sales, and repacking units
- Import/export licensing and international product registration
- eCTD preparation for NDA, ANDA, IND, and DMF submissions
- Labeling and artwork approval under Rule 96
- Regulatory response handling and audit support
- DSIR, FSSAI, WHO-GMP, and Free Sale Certificate assistance
- Market entry planning and regulatory gap analysis
- Trademark, NSQ handling, and court-compliant submissions
Why Choose Us
Regulatory Expertise
Years of hands-on experience in navigating Indian drug laws and compliance frameworks.
Complete Documentation Support
We handle end-to-end paperwork — from preparation to submission and follow-up.
Government Liaison
Strong working relationships with DCA, CDSCO, and DCGI for smooth regulatory processes.
Proven Success Rate
High approval rates for licenses, product registrations, and regulatory audits.
Skilled Professionals
A dedicated team of pharma experts with deep domain knowledge and precision.
Fast Market Access
Helping you launch products quickly and compliantly in both domestic and global markets.