The API
partner of
choice
for the world's

leading pharma companies.

Here are 8 reasons why:

Six mega-capacity manufacturing plants.

Ready to scale up your production.

  • Dedicated facilities for ARVs, Peptides, and Iron Complexes.
  • Multipurpose production blocks for manufacturing APIs with variable demand.
  • Specialised drying techniques to ensure specific quality standards, including polymorph.
  • Over 45 GMP audits by global regulatory agencies since 2017.
  • Expertise in scaling up and expanding production capacities.
  • Unique capabilities to meet diverse particle size specifications.
  • Specialised drying techniques to ensure specific quality standards, including polymorph.
  • Over 45 GMP audits by global regulatory agencies since 2017.
  • Setting up a cGMP pilot plant and kilo-lab.
  • Developing a dedicated containment facility for HPAPls.
  • High-quality manufacturing standards combined with a highly skilled workforce.

World-class
R&D capabilities

with leading scientists working for you to deliver consistent value across API development cycle.

R&D Capabilities

  • Novel polymorphs screening and development
  • Complex APIs — Peptides, HPAPIs, Iron compounds, Biocatalysts (Enzyme based)
  • Novel, cost-effective, efficient, and eco-friendly process development

R&D Capabilities

  • Dedicated Kilo Lab — Expertise in tech transfer and scale-up
  • First to market with the majority of novel ARVs

Technological Capabilities

  • SYNTHETIC CHEMISTRY
    - High pressure reactions
    - Hydrogenation
    - High temperature reactions
    - Cryogenic reactions

Technological Capabilities

  • SYNTHETIC CHEMISTRY
    - Azide reactions
    - Pyrophoric reactions
    - Other reactions

Technological Capabilities

  • DRYING TECHNOLOGIES
    - Spray dryer
    - Spin flash dryer
    - Micronisation
    - Spherical dryer
    - Pressure swing adsorption system

Technological Capabilities

  • PEPTIDES
    - Solid and liquid phase synthesis
    - Preparative HPLC
    - Lyophilisation
  • COE LAB
    - For nitroso and azido impurities

One of the largest CMOs in India

with best-in-class systems and processes. To secure unmatched quality and timely solutions for your success.

  • Integrated quality and compliance organization
  • Automated process across Manufacturing, Quality, and Learning & Development functions
  • Strong commitment to EHS (Environment, Health, and Safety)

Facilities certified by US FDA, EU GMP, WHO

and other leading international regulatory bodies. To ensure the highest standards of quality in API production.

Partnering with the world's leading pharma companies

Over 500 customers in 80 countries.

  • Our customers include marquee companies such as GSK, Sandoz, and Bayer, among others
  • We have strong supply relationships with leading companies like VIATRIS

A leading API producer with over 280 DMFs

and 40 more in the pipeline. Our diversified portfolio across 20 therapeutic areas is all set to expand yours effortlessly.

Key therapeutic areas.

Anti-viral: 5+
Anti-diabetic: 10+
CNS: 20+
Retroviral: 18+

Anti-neoplastic: 17+
Anti-hypertensive: 20+
Proton Pump Inhibitor: 4+
Cardiovascular: 3+

DMF/CEP Submission

US: 231
EU: 133
Japan: 37
Canada: 72

Korea: 25
China: 13
Brazil: 27
Others: 62

Optimising efficiency to optimise results

By focusing on operational efficiency, implementing continuous process improvement, and partnering with established suppliers, we deliver exceptional value.

Operational efficiency

  • Time cycle reduction
  • Solvent recovery and optimisation
  • Capacity and scale enhancement
  • Equipment optimisation

Raw Material

  • Robust qualification process
  • Geographical risk mitigation
  • Development of alternate sources
  • Backward integration

Process improvement

  • Alternate/new development
  • Process optimisation
  • Redevelopment of test methods
  • Strong tech transfer

Caring for people and the planet

We’re committed to the highest environmental, health and safety standards - fostering a safe and sustainable future for all.

Environment

  • All 6 manufacturing sites are ISO 50001 compliant
  • Our manufacturing operations are ISO 14001 compliant
  • EcoVadis assessment completed

Environment

  • All sites are equipped with 'Effluent Treatment Plant' systems for 'Zero Liquid Discharge'
  • Continuous process improvements to reduce effluent load

Health

  • Pre-employment and periodical medical examination
  • Workplace monitoring and surveillance to avoid any unsafe practices
  • Closed transfer systems

Safety

  • ISO 45001 compliant manufacturing operations
  • State-of-the-art 'Process Safety Laboratory': RCIe, TSU, Powder Testing - MIE, LIT

Safety

  • Full-time member of PSCI (Pharmaceutical Supply Chain Initiative)
  • Received the 'Five-Star Rating' and 'Sword of Honor' from the British Safety Council
For our full product list, click here

Unlock the advantages
of partnering with
Matrix Pharma Corp.

Enter your details below and we'll get in touch with you.