Where Markets Meet Momentum

World-Class Manufacturing & Research Facilities

Manufacturing Units & Portfolio

With manufacturing sites approved by the EU and US FDA, Medicamen is well-positioned to serve regulated markets. They serve as the foundation for Medicamen’s expanding role in global product development and innovation.

Strategically located R&D and manufacturing facilities are the backbone of Medicamen’s ability to scale, uphold uncompromising quality, and move with agility across its pharmaceutical business. This integrated footprint positions the Company to meet global demand with speed and confidence, while maintaining the highest standards of safety, precision, and performance.

Location 1 Bhiwadi Facility

Bhiwadi, Rajasthan

Facility Details

  • 21,000 sq. ft. area
  • Six-block contemporary facility for general formulations
  • Dedicated R&D block for formulation

Certifications

  • EU GMP (Greece)
  • WHO GMP
  • ISO
Location 2 Haridwar General Facility

Haridwar Unit I, Uttarakhand (General)

Facility Details

  • 210,000 sq. ft. area
  • Focused on general formulations across finished dose forms
  • World-class integrated quality control lab

Certifications

  • WHO GMP
Location 3 Haridwar Oncology Facility

Haridwar Unit II, Uttarakhand (Oncology)

Facility Details

  • 350,000 sq. ft. area
  • State-of-the-art facility dedicated to oncology
  • Specialized lines for highly potent and lyophilized formulations

Certifications

  • US FDA Approved
  • WHO GMP
Location 4 R&D Facility at Bhiwadi

R&D Facility at Bhiwadi (Rajasthan)

Facility Details

  • 12,000 sq. ft. operations with ₹40 Cr. investments
  • 60 scientists & pharmacists driving new formulations
  • Approved by the Department of Scientific & Industrial Research (DSIR)

Certifications

  • DSIR Approved
Location 5 Agro-chemical Facility at Dehradun

Agro-chemical Facility at Dehradun (Uttarakhand)

Facility Details

  • Annual capacity of 1,450 MT
  • 95% capacity utilization across formulations
  • Skilled workforce of 200+ associates

Certifications

  • ISO 9001:2015
Location 6 Pharma API Facility at Dahej-II

Pharma API Facility: Onco & Non-Onco at Dahej-II (Gujarat)

Facility Details

  • US FDA-approved facility
  • Spread across 50,000 sq. ft. with 30 KL reactor capacity
  • Dedicated lines for both oncology and non-oncology production
  • Expansion underway with a dedicated R&D block

Certifications

  • US FDA Approved
Location 7 Agro & Specialty Chemical Facility at Dahej-III

Agro & Specialty Chemical Facility at Dahej-III (Gujarat)

Facility Details

  • Commercial operations commencing September 2024
  • 2,000 MT per annum capacity designed for insecticides & fungicides
  • Purpose-built for formulation manufacturing and scale-up

Certifications

  • Designed for ISO 9001:2015

International Certifications

Our commitment to excellence is validated by globally recognized certifications and regulatory approvals.

WHO-GMP Certified

World Health Organization Good Manufacturing Practices certification ensuring international quality standards.

ISO 9001:2015

International Organization for Standardization quality management system certification.

FDA Approved

United States Food and Drug Administration approval for manufacturing and quality systems.

EU GMP Certified

European Union Good Manufacturing Practices certification for export to European markets.

Experience Excellence

Schedule a facility tour to witness our world-class infrastructure and quality systems firsthand. Discover how we maintain the highest standards in pharmaceutical manufacturing.

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