OUR CONTRACT PHARMACEUTICAL SERVICES

Company Overview

CONTROLLED SUBSTANCES & DRUG PRODUCT

Over ten years of extensive development and manufacture experience converting controlled substances.

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At Quay Pharmaceuticals, we have over 10 years of extensive development and manufacturing experience converting controlled substances into a variety of different dosage forms.

Therefore, you can have complete assurance in our proficiency to deliver your project with controlled substances quickly and efficiently.

Our Deeside facility is fully licensed by the UK Home Office to possess, produce and supply controlled substances covering schedules I to IV (parts I and II). As required by the Home Office, the Deeside site has the required physical security processes as well as tightly controlled procedures, administrative controls, and accountability processes that are carried out by experienced, highly qualified staff.

Quay has worked with both synthetic and plant extract controlled materials and arranged import or export licences with the UK’s Drugs and Firearms Licensing Unit as required to move controlled substances or products across state boundaries.

Examples of Quay’s development of controlled substances:

  • Schedule I controlled substance for clinical trial use
  • Schedule II controlled substance for commercial use
  • Schedule IV controlled substance for Specials Supply
Your Dedicated Contacts
David Blum
Managing Director (Israel)
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Michael Kruidenier
Head of Business Development
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Our Pharmaceutical Services

Preclinical Formulation

Robust formulation development strategies tailored to the characteristics of each individual API.

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Pharmaceutical Preformulation

Analysis of Active Pharmaceutical Ingredients (APIs), including those that present particular challenges.

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Pharmaceutical Formulation Development

Dosage form optimisation for a wide range of product types including those that have poor solubility or bioavailability.

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Analytical Services

Analytical specialists working alongside our formulation and manufacturing teams which provide expert advice.

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Phase I Clinical Manufacturing

Early clinical formulations and clinical manufacturing of First in Human trials and clinical evaluations of your API.

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Phase II & III Clinical Manufacturing

Fully equipped and accredited to manufacture a wide range of products for Phase II and small-scale Phase III trials.

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Commercial Manufacture & Packaging

MHRA licensed to include commercial manufacture. Services include contract packaging and assembly...

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Controlled Substances

Over ten years of extensive development and manufacture experience converting controlled substances into a variety of different dosage forms.

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Clinical Trial Supply

Complete range of clinical trial supply packaging for solid and liquid dosages. Despatched with full QP release certification.

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Live Biotherapeutics Drug Delivery

One of the few companies licensed for the clinical manufacture of live biotherapeutics products.

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Orphan Drugs

Perfectly equipped to deliver an Orphan Drug molecule from preclinical and formulation development to small scale commercialisation.

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Specials Manufacturing

One of the limited number of contract manufacturers who hold an MRHA license for the manufacture and supply of ‘specials’.

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Let's Talk Project Success

Talk directly to the Quay staff - Our dedicated team leaders are ready to listen and help with your project.

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