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Manufacturing Facilities

Technical Aspects

Martin Dow Group is an innovation-driven group committed to providing a broad range of high-quality medicines and formulations that deliver on the promise of better patient outcomes.

Our capabilities span a wide range of therapeutic areas, and our EU GMP compliant manufacturing facilities are outfitted with robust technologies dedicated to providing consistent quality and developing high-performing Pharmaceutical and Nutraceutical products that excel in terms of efficacy and cost-effectiveness.

All of our international manufacturing facilities are certified by ANSM, Synadiet, Ecocert, DG CCRF, and Agriculture Biologique, and adhere to the strictest international standards in order to provide results that satisfy our partners’ and consumers’ unmet needs.

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Quality

Creating distinction for life has always been at the core of our business practices at Martin Dow. To attain this distinction, we have a quality-driven approach from manufacturing to delivering high-value products to our consumers and partners.

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New Product Development

We have a dedicated new product development (NPD) Lab, a state-of-the-art facility recognized by the local drug regulatory body. It is equipped with the latest equipment for manufacturing, packaging, and testing new products.

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Our Standards

At Martin Dow, we invest in cGMP compliant manufacturing technologies and state-of-the-art facilities built to international standards.

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Quality Management System

  • We maintain a well-established quality management system (QMS) for safe, reliable, and consistent quality products
  • We maintain a well-established quality management system (QMS) for safe, reliable, and consistent quality products
  • State-of-the-art qualified and calibrated equipment is available in quality control for analysis
  • We implement serialization barcoding for Martin Dow Limited products as a best practice
  • 24/7 temperature and humidity monitoring of all storage areas via data loggers
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Control and Validation

  • Relevant guidelines are being reviewed for WHO pre-qualification and PIC/s certification
  • Relevant guidelines are being reviewed for WHO pre-qualification and PIC/s certification
  • A well-defined supplier selection process, including an approved supplier list (ASL), is in place
  • Annual product review is performed as per WHO guideline
  • Advanced ERP system is in place – SAP version 4.0 HANA throughout the production processes
  • Stability studies are performed in full compliance with ICH guidelines
  • Impurities testing and process and packaging validation are performed for each product
  • Continuous improvement is an integral part of quality culture and has been embedded into the processes
  • Change control CAPA systems are monitored and implemented
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Connect With Us

For information and queries:

+92 21 111 111 634

For information and queries:

+92 21 350 605 41