OUR CONTRACT PHARMACEUTICAL SERVICES

Company Overview

MHRA & US FDA INSPECTED FACILITIES

We are licensed and approved by the MHRA, and have been inspected by the FDA.

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Quay Pharma is licensed and approved by the MHRA, and has been inspected by the FDA for the following:

Under MIA(IMP) 20300, Quay Pharma is licensed for the manufacture and packing of:

  • Hard shell capsules
  • Liquids
  • Semi-solids
  • Suppositories
  • Tablets
  • Other medicinal products such as; cytotoxic materials, steroids, sachets and live biotherapeutics

Under MIA 20300, Quay Pharma is licensed for the commercial manufacture and packing of:

  • Hard shell capsules
  • Liquids
  • Semi-solids
  • Suppositories
  • Tablets
  • Other medicinal products such as; cytotoxic materials, steroids, sachets and live biotherapeutics

Under MS 20300, Quay Pharma is licensed for the ”specials” manufacture and packing of:

  • Hard shell capsules
  • Liquids
  • Semi-solids
  • Suppositories
  • Tablets
  • Other medicinal products such as; cytotoxic materials, steroids, sachets and live biotherapeutics

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