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Pharmaceutical Manufacturer

Glatrix: A Leading Pharmaceutical CDMO

Glatrix is a premier Contract Development and Manufacturing Organization (CDMO) specializing in the development and production of high-quality pharmaceutical products for clients worldwide. We offer a comprehensive suite of services, from early-stage formulation development to commercial-scale manufacturing.

Core Capabilities

  • End-to-End Product Development: We provide complete solutions, from concept to commercialization, including formulation development, process optimization, and scale-up.
  • Intellectual Property: We own the intellectual property for several manufacturing processes, ensuring competitive advantage for our clients.
  • Regulatory Expertise: Our team assists with the preparation and filing of regulatory dossiers in India and international markets, navigating complex regulatory landscapes.
  • Comprehensive Services: Our offerings encompass formulation R&D, analytical testing, stability studies, and other critical services to support the entire product lifecycle.

Research & Development Excellence

Our dedicated R&D unit drives innovation across key areas, including:

E.g., Novel Drug Delivery Systems, Biologics Development] Controlled Release Formulations, Solid State Chemistry.

This Revised Version:
  • Emphasizes Key Strengths: Highlights your core capabilities as a CDMO, such as end-to-end solutions, IP ownership, and regulatory expertise.
  • Provides a Concise Overview: Summarizes your services in a clear and impactful manner.
  • Focuses on R & D: Clearly outlines the key areas of expertise within your R&D unit.

Research and Development

Our Research and Development (R&D) Unit excels in four key areas of expertise, driving continuous innovation and ensuring groundbreaking solutions in product development.

Quality Assurance

Compliance, testing, and continuous improvement are at the core of our operations, ensuring the highest standards for our products.

Committed to Regulatory Compliance

  • Regulatory Strategy Development
  • Regulatory Audits and Assessments
  • Global Regulatory Approvals
  • Dossier Compilation and Submission Management
  • Adherence to Good Manufacturing Practices (GMP)

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Customer Satisfied

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FSSAI Approvals

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Billion Units

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Commercialized Formulations

Our Manufacturing Capacities are as Follows

S. No. Medicine Per Day
1 General Section Tablets 6 Millions
2 General Section Capsules 1 Millions
3 Nutra Section Tablets (Dedicated Facility) 5 Millions
4 Nutra Capsules 1 Millions
5 ⁠Nutra Automatic Liquid Filling Line 5 Lakh Bottles
6 ⁠Nutra Automatic Tablet/Capsule Counting Line 5 Lakhs
7 ⁠Nutra Sachets 5 Millions
8 ⁠Nutra Protein Powder 1 Million
9 Nutra Drops 5 Millions
Our Work Prcocess
Our Expertise

Manufacturing and Quality Assurance

Manufacturing

Precision and dedication are the hallmarks of our commitment to excellence, reflected in every product we create.

Innovation

We are driven by an unwavering pursuit of creativity, consistently pushing boundaries and shaping the future.

Quality

Our steadfast commitment to uncompromising standards guarantees satisfaction for our customers.

Regulatory

We adhere to the highest ethical and legal standards, consistently fulfilling our commitment to compliance and integrity.

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