VIRTUAL TOUR
OUR SERVICES

We provide a comprehensive range of pharmaceutical services to support every stage of drug development and commercialization. Our offering includes formulation and Analytical Development for custom-tailored drug products, Co-development partnership Opportunities for formulations, CDMO services that streamline drug manufacturing at all stages, In/Out licensing solutions to extend product's reach into new markets and Contract Manufacturing (CMO) in production scale of your choice with a wide range of dosage forms and packaging services through Tech-transfer. Whether you are developing a new drug or scaling an existing one, we offer the expertise and resources to bring your vision to life.

Equipped with the state-of-the-art R&D infrastructure, BioMatrix offers full spectrum of services tailored to the pharmaceutical industry's needs.

Contract Development & Manufacturing Organisation (CDMO)

From research and development to full-scale production of non-infringing formulations, BioMatrix provides end-to-end Contract Development and Manufacturing Organisation (CDMO) services. We offer flexible solutions to meet both small-scale and large-scale production needs.

  • Research and Innovation: Cutting-edge research focused on breakthrough drug solutions.
  • Drug Development: Full-cycle drug development, from concept to product.
    • Formulation Development:Tailored solutions ensure that drugs are developed with the highest standards for efficacy, stability, and safety.
    • Analytical Development:Standardized and custom methods to
      develop and validate the quality of pharmaceutical products.
  • Pre-Manufacturing Stages: Stability testing, validation, and regulatory compliance preparation.
  • Commercial Manufacturing: Scale-up capabilities to meet commercial demands with flexibility.
Image

Advantages: Our CDMO services allow clients to focus on their core competencies while we handle the complexities of development and manufacturing. We offer flexible solutions to meet both small-scale and large-scale production needs.

We offer expertise in developing formulations for different dosage forms from Lab to Life Production Capabilities:

Batch Capacity
Laboratory Scale Solids: 200 gm to 2 Kg
Liquids: 500 ml to 10 Liters
Exhibit Scale Solids: 5 Kg to 30 Kg
Liquids: 120 Liters to 300 Liters
Commercial Scale Solids: 30 Kg to 2000 Kg
Liquids: 300 Liters to 4000 Liters

Specializations:

  • Dosage Forms: Expertise in Tablets, Capsules, Liquids, and more.
  • Customization: Tailored formulation to meet specific therapeutic and market needs.
  • Stability Studies: Comprehensive accelerated and to long-term stability studies to ensure shelf life.
    Study Type Storage Condition Storage Period
    Accelerated Temperature: 40°C ± 2°C and RH: 75% ± 5% 0, 01, 03 and 06 Months
    Intermediate Condition Temperature: 30°C ± 2°C and RH: 65% ± 5% 0, 03, 06, 09 and 12 months
    Long Term Temperature: 30°C ± 2°C and RH: 75% ± 5% 0,03,06,09,12,18,24 and 36 months
    Long Term Temperature: 25°C ± 2°C and RH: 60% ± 5% 0,03,06,09,12,18,24 and 36 months
Contract Manufacturing Organization (CMO)

Equipped with state-of-the-art R&D infrastructure, BioMatrix offers these services to customers:

BioMatrix Healthcare is fully equipped to offer you international standard pharmaceutical Contract Manufacturing services in production scale of your choice in a range of dosage forms and packaging options. Our portfolio of products includes a diverse variety of life-saving drugs like Tablets, Capsules, Liquid and Dry Powder for Suspension. We leverage state-of-the-art manufacturing facilities to deliver high-quality drugs that meet the rigorous demands of the pharmaceutical industry.

Our expert team ensures that all intellectual property and production methods are safeguarded and implemented flawlessly.

  • Technology Transfer: We support long term supply agreements through Technology Transfer.
  • Registration Batches: Production of batches for regulatory submission and approval.
  • Commercial Manufacturing: High-volume manufacturing to meet commercial demands.
Image
Technology Transfer

BioMatrix Healthcare provides seamless Technology Transfer services, allowing for the smooth transition of innovations from the research stage to commercial manufacturing.

Why Choose Us: We provide reliable support throughout the technology transfer process, ensuring that your research outcomes are turned into successful products. Our expert team ensures that all intellectual property and production methods are safeguarded and implemented flawlessly.

What We Offer:

  • Bundled Services: Full-spectrum services from initial R&D to final product adaptation.
  • Seamless Handover: Coordination between research, development, and production to ensure a smooth transition.
  • Collaboration: We work closely with your team to ensure that the technology is transferred efficiently and effectively with minimal disruption.
Formulation Development

At BioMatrix, our Formulation Development services ensure that drugs are developed with the highest standards for efficacy, stability, and safety. We offer expertise in developing formulations for different dosage forms.

Batch Capacity
Laboratory Scale Solids: 200 gm to 2 Kg
Liquids: 500 ml to 10 Liters
Exhibit Scale Solids: 5 Kg to 30 Kg
Liquids: 120 Liters to 300 Liters
Commercial Scale Solids: 30 Kg to 2000 Kg
Liquids: 300 Liters to 4000 Liters
  • Dosage Forms: Expertise in Tablets, Capsules, Liquids, and more.
  • Customization: Tailored formulation to meet specific therapeutic and market needs.
  • Stability Studies: Comprehensive testing to ensure long-term stability and shelf life.
In/Out Licensing
BioMatrix Healthcare provides In/Out-Licensing opportunities for pharmaceutical companies looking to leverage pre-developed and market-ready products.
    Key Areas of Licensing:
  • Innovative drug formulations.
  • Pre-formulated products in various therapeutic areas.
  • Products ready for commercialization in specific markets.
Regulatory Support

BioMatrix’s vibrant Regulatory Affairs (RA) team is fully equipped to develop regulatory strategy and manage compliance, risks and dossier submissions across the globe. They provide expert regulatory support to ensure compliance with international standards and help navigate the approval process. Our team works closely with regulatory bodies to ensure that all products are in compliance with local and international regulations. We assist in regulatory submissions and certifications, ensuring a smooth path to market.

RA Team Offers:

  • Product / dossier development in CTD format
  • Dossiers Compilation & Due diligence
  • EU CTD Dossier Filing Through National, DCP & MRP Procedure
  • Packaging Design and development which meets both regulatory and market demands

Services Provided:

  • FDA Compliance: Meeting U.S. FDA requirements for drug development and manufacturing.
  • EMA Compliance: Adherence to European Medicines Agency regulations.
  • Global Market Compliance: Expertise in complying with regulatory authorities in various regions such as South America, Africa, and Asia.
Business Models
  • Contract Manufacturing Organization (CMO)
  • Contract Development & Manufacturing Organisation (CDMO)
  • IN/OUT LICENSING
Logo