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MHRA & US FDA Inspected

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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

For all sales enquiries, call us on +44 (0)1244 837000 and a member of our Business Development team will be happy to help. Alternatively, fill out a quick form on our contact page.

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