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Commercial Packaging

Analytical Laboratory Services

PCI provides fully audited, in-house laboratories in both our European and North America locations offering a range of analytical services to support clients in the development and commercialization of new medicines.


DSCSA Serialization & Anti-counterfeiting
Deadline Update

DEADLINE FOR COMPLIANCE HAS ARRIVED, WE CAN HELP!

We are industry leaders in product security for global medicines with significant Serialization and Anticounterfeiting technologies. Find out how our experienced teams can work with you to understand your exact requirements to ensure your product’s integrity and protect patient safety.




Staffed with expertly qualified analytical chemists, trained and accredited in the most comprehensive laboratory standards, we provide a complete range of resources and responsive services at each stage of the product lifecycle across a wide variety of dosage forms.

Our analytical services include:

  • Stability testing
  • ID testing
  • Import testing
  • Import release testing

Our state-of-the-art facilities feature best in class and fully GMP and ICH compliant analytical equipment enabling our teams to perform simple ID testing and analytical method transfers, through method development and validation, to EU product release and ICH stability testing, ensuring data reliability and regulatory compliance.

Our facilities also include HEPA filtered air handling systems for the analysis of cytotoxic, teratogenic and uncharacterized products, a darkroom for the analysis of light sensitive products, and the capabilities to work with Schedule II-IV controlled substances.

Analytical services are offered on a stand-alone basis or in conjunction with our clinical, commercial and QP services to facilitate a seamless transmission through the drug development cycle.

Our dedicated team of specialists will be happy to discuss our QP Services. Contact us on +1 779-774-1428 (US) or +44 1495 713 633 (UK) or email sales@pciservices.com


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