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QP Services & Support

We can work with you to assess and facilitate Good Manufacturing Practice (GMP) compliance of operations at both your and any partner facilities from Active Pharmaceutical Ingredient (API) Manufacture to Commercial manufacture, testing and packaging.  ​

We are able to conduct any necessary QP audits and provide audit reports as required. We will work with the facilities to close out any observations and then we will provide an audit certificate to support your QP Declaration and/or external vendor management programme.   

Our QP Experience Covers:

  • Eligible to act as a Qualified Person (QP) via the permanent provisions since March 2014
  • Over 18 years’ experience in the pharmaceutical industry across key positions in quality assurance
  • Extensive experience in sterile and non-sterile dosage forms for clinical Trial, Commercial and Special patient supply.
  • Worldwide audits of manufacturing sites and supply chain networks, third party organisations, affiliates and contractors to EU GMP requirements.
  • Experienced in a variety of functions including contract manufacturing and packaging, aseptic, terminal sterilisation, solid and liquid dose manufacture, specials, supplier/client audits and QC testing/stability.
Qualified Persons are a requirement under 2001/83/EC and 2001/82/EC.

We hold MHRA licenses for the secondary packaging & assembly of human and veterinary medicines.

We also hold ISO 13485 accreditation for the assembly and packaging of medical devices and in addition we hold ISO 9001 accreditation.

Let's talk

If you’re looking to reduce costs without compromising quality, flexibility and service, we believe Springdew offers you a genuine alternative.

Talk to our team on 01639 849 676 or email sales@springdew.co.uk or fill in the form and we will get back to you as soon as we can. Office hours are Monday to Friday 09:00 to 17:00.

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About us

Springdew Ltd provide contract packing services across pharmaceutical, healthcare, veterinary and medical device markets.

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