BioMatrix Healthcare Pvt. Ltd.

Established in the year 2007, with a thought of “Supporting Life Worldwide”. With headquarter at Ahmedabad, currently we are into 100% export business. We have committed ourselves to provide affordable and innovative healthcare globally.

Financial Growth

From last five years the company has posted robust growth of 33% CAGR. The company has achieved its first dream milestone of INR 1000 millions Annual Revenue in FY 2018-19.

Business Expansion
  • Strong presence in 21 countries of Africa and CIS region
  • Ongoing registrations in 10 countries of the Francophone region
Product Basket (Portfolio)
  • 1000+ Products registration
  • 450+ Products under registration

Manufacturing Facility

BioMatrix has State-of-the-Art Oral solids, Liquid and Dry syrup manufacturing facility with WHO-GMP, EU-GMP accreditation and US-FDA, UK-MHRA & ANVISA compliance.

With this State-of-the-Art manufacturing facility, BioMatrix will accelerate its growth in the existing international markets and shall expand its wings further across the globe.

 

Manufacturing Capacities:
  • 5 Billion Tablets/Annum
  • 1 Billion Capsules/Annum
  • 24 Million Bottles of Liquid/Annum
  • 18 Million Bottles of Dry syrup/Annum
Experience over the years

Vast experience of Management in Domestic & International Market had been the driving force that leads our team forward.

Domain Expertise

With decades of experience, the team has expertise to innovate and evolve customer driven marketing strategies to sustain market leading position in this competitive era.

Trust Of Customer & Associates

Extensive Experience, Core Competency & Strong Business Ethics has made BioMatrix earn trust of all its Customers & Associates.

Milestone

2007 - 2013

  • Establishment of Biomatrix in a modest setup in Ahmedabad.
  • Over 100 products registered!

2018

  • A year of surpassing INR 100 million turnover, and also registering 250 products

2020

  • Commissioned a state of the art, WHO-GMP compliant manufacturing facility

2022

  • Commenced Operation in Francophone Countries
  • 800+ Product Registrations

2023

  • Accorded the status of  3 Star Export House
  • Established Research and Development (R&D) Center to Develop Innovative Product & PRocess

Future Roadmap

2024

  • UK-MHRA, TGA & Health Canada Approval for Manufacturing Plant
  • To commence Operations in Europe, Central, South, and Latin America

2025

  • To establish API Manufacturing Unit
  • To commence Domestic Operations

2026

  • Establishment of New Manufacturing Facility for Injectables

2027

  • USFDA Approval for Manufaturing Plant

Our Global Reach

Certification

World Health Organisation-GMP

Europe-GMP

Medicines Control Authority of Zimbabwe

Ethiopian Food & Drug Authority

Tanzania Medicines and Medical Devices Authority

National Drug Authority UGANDA

Food and Drug Authority GHANA

Pharmacy & Poisons Board | KENYA

National Regulatory Authority for Medicines of Mozambique (ANARME)

Pharmacy and Medicines Regulatory Authority MALAWI

Congolese Pharmaceutical Regulatory Authority (ACOREP) - DR CONGO

Ministry of Health CAMBODIA

Ministry of Public Health & Population | YEMEN

Three Star Export
House

Why Choose Us

i

Certified

WHO-GMP, EU-GMP Manufacturing Facility

Compliance

US-FDA, UK-MHRA and ANVISA

Star

Three-Star Export House

15 +

Years of Experience

30 +

Countries we are present in

l

1000 +

Product Registrations

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