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Clinical Services

We specialise in the clinical manufacture of non-sterile oral solutions and provide a range of clinical trial manufacturing services. We offer a full range of clinical packaging and distribution services, and we are trusted by some of the world’s largest pharmaceutical companies and sponsors for the manufacturing, packaging and distribution for all phases of drug development.

As experts in the life sciences industry, we understand the unique challenges faced by both emerging biotech startups and established global pharmaceutical companies. Our flexible solutions can be tailored to meet the specialised needs of organisations of any size or stage of development.

Here at Wasdell we have the full quality infrastructure in place and can provide Qualified Person Release Certification to meet the QP certification requirements for clinical trials, as well as QP EU release for imported IMPs. In this way, we can help our customers ensure they comply with the Clinical Trial Directive 2001/20/EC.

Our clinical trial manufacturing capabilities are comprehensive and state-of-the-art, allowing us to support clinical trial sponsors with all their investigational medicinal product (IMP) needs.

  • We can manufacture IMPs in the recommended dosage form as well as placebos to the highest quality standards.
  • In addition, we can source comparators, non-investigational medicinal products, and any necessary auxiliary medicinal supplies required for your trial.
  • Our team performs release testing on the batches and conducts stability studies for IMPs while adhering to BP/EP standards to ensure quality and consistency.
  • We have an on-site analytical laboratory equipped for identity testing of materials.
  • For products requiring sterilisation, we offer dry heat sterilisation capabilities. All material sampling is performed in our Grade C certified facilities.


To round out our full-service offerings, we provide a complete range of clinical packaging and distribution services to seamlessly get your clinical trial supplies to sites across Europe. With our extensive capabilities and commitment to quality, you can trust us as your partner to expertly handle all your clinical trial manufacturing needs.

Our comprehensive clinical packaging and distribution services are designed to efficiently and effectively meet all your trial needs.

  • We offer convenient late-stage customisation labelling services that reduces inventory costs, eliminates repackaging work, and prevents waste.
  • Whether your trial requires an open, double-blinded or a late-stage approach, our experienced clinical trial packaging professionals can accommodate it.
  • We’re able to de-blister, de-bottle, or over-encapsulate tablets and capsules, and can pack pharmaceuticals in bottles, blisters, sachets, tubes and wallets – whatever your study demands.
  • Our label design capabilities span all European languages plus Russian and Chinese, ensuring your trial materials are clearly marked in any target market.
  • When your study concludes, we’ll handle all the post-study returns, accountability and destruction.
  • With our temperature-controlled worldwide shipment, storage and distribution capacity, your clinical trial pharmaceuticals will remain in optimal condition from start to finish.
  • We also audit the complete supply chain to meet Annex 13 and 16 requirements and support your subsequent commercialisation efforts. For added assurance, we provide Qualified Person Release Certification to satisfy QP certification requirements for clinical trials, as well as QP EU release for imported IMPs, helping you comply with the Clinical Trial Directive 2001/20/EC.


With our full-service capabilities and attention to detail, you can focus on your core research knowing your clinical packaging and distribution needs are in expert hands.

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