Our Vision

To be a trusted global leader in regulatory consulting, empowering industries to achieve compliance and bring safe, high-quality products to market efficiently.

Our Mission

To provide exceptional, reliable, and innovative regulatory solutions, simplifying complex processes while ensuring compliance with industry standards and regulations.

Our Values

We take full responsibility for the solutions we provide, ensuring our clients achieve their compliance goals seamlessly.

About Us

Ved Pharma Consultancy.

Ved Pharma Consultancy is a leading regulatory consulting firm, specializing in providing comprehensive services to the pharmaceutical, cosmetic, and nutraceutical industries. We assist businesses in navigating the complex regulatory landscape by ensuring compliance with the Central Drugs Standard Control Organization (CDSCO) and Drug Controller General of India (DCGI) standards. Our expert team supports clients in obtaining necessary approvals and licenses, helping them bring safe and effective products to market.

Why Choose Us?

Ved Pharma Consultancy combines expert guidance, efficient processes, and tailored solutions to simplify regulatory compliance, saving you time and resources. We ensure seamless approvals, aligning with global standards for market success.

  • Unparalleled Expertise
  • Streamlined Processes
  • Compliance Focus
  • Personalized Solutions
  • Client-Centric Approach
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Have Questions? Call Us Today!

If you have any inquiries about our services or need assistance with regulatory approvals and compliance, our expert team is here to help. Contact us now, and let Ved Pharma Consultancy be Your Trusted Partner in Regulatory Compliance in navigating the regulatory landscape with ease and efficiency!

Exactly What Facilities We Provided

Regulatory Approvals

Assistance in obtaining CDSCO/DCGI approvals for pharmaceutical, cosmetic, and nutraceutical products, including IND, SND, FDC, and more.

Licensing Services

Support for manufacturing, import, export, and wholesale licenses, along with renewals and market standing certificates.

Clinical Trial Management

Comprehensive guidance for clinical investigations, including BA/BE studies, toxicity studies, and global trial management.

Documentation & Dossier Preparation

Expert preparation of regulatory dossiers for national and global submissions, ensuring compliance with industry standards.

SUGAM & NSWS Account Setup

Assistance with account creation for regulatory platforms like SUGAM and NSWS for smooth regulatory submissions.

Plant Setup & QMS Compliance

End-to-end guidance for plant establishment, including quality management system (QMS) data preparation and regulatory alignment.

Our Clients