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Martin Dow | Creating Distinction for Life
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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 GMP-compliant manufacturing facilities are outfitted with robust technologies dedicated to providing consistent quality and developing high-performing Pharmaceutical products that excel in efficacy and cost-effectiveness.

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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