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Manufacturing Facility

Manufacturing Facility

INFORMATION

PLANT FACILITY

  • MEDPHARMA is headquartered in Sharjah, United Arab Emirates
  • MEDPHARMA has world class facility established according to the international adopted policies and the highest standards of current good manufacturing practices
  • MEDPHARMA manufacturing facility and related premises are periodicallt audited by licensors and health authorities.
  • MEDPHARMA adheres to international quality, security and production standards and aim to work with our distributors and customers worldwide to achieve the evolving expectations and requirements and constantly improve products and services for the benefit of patients.
  • MEDPHARMA is proud to consistently increase in product development investment to expand our product range acriss anti-infective, dermatology and NSAIDs (analgesics).
  • MEDPHARMA employs over 130 people and all products are produced completely in the UAE.
  • MEDPHARMA is a dependable partner for multinational companies in their search for new opportunities by granting manufacturing rights under license or partnering for the marketing and distribution of their products in the MENA region.
  • MEDPHARMA cover the manufacturing and packaging of solid, semi-solid, cephalosporin and OTC.
  • MEDPHARMA all local and regional health authorities regulations such as GMP, GSP, GDP, as well as licensors requirements such as ISO 9001:2015, ISO14001:2015 and ISO 45001:2015.
  • MEDPHARMA strictly adhere to a global Quality Management System with strict monitoring through all stages of the manufacturing and packaging process.

QUALITY

  • Quality Assurance (QA) is an integral part of Medpharma operations with a soul objective in ensuring Quality complaince with the applicable GMP regulations as well as fostering the culture of continuous training and process improvement. Medpharma processes are thoroughly described in an Integrated Management System and compliant with UAE, Saudi Arabia and GCC GMP regulations. Further, Medpharma site is certified for ISO 9001:2015 (Quality Management SYstem), ISO 1400:2015, ISO 45001:2015 from a credible certifying body.
  • Quality Control is applied at all phases of operation starting from raw material procurement until final receipt of finished products at our customers sites.
    • Qualification, inspection, testing, monitoring and release of raw and packaging materials, in-process and finished products.
    • Only procuring raw materials from referenced pharmacopeia suppliers and US FDA/EU certified sources for active pharmaceutical ingredients.
    • Microbial environmental monitoring during all phases to ensure that product safety and efficacy remain intact.

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