Qualified Persons (QPs) deliver a vital role in bringing new products to market. Our highly experienced team ensures that clinical studies not only meet the most vigorous standards but also run smoothly, seamlessly, and cost-efficiently.
Our team of qualified persons assume responsibility for all stages of the process, safeguarding patients including the audit of the supply chain for GMP compliance in addition to certification of products for use in clinical trials.
At PCI, our QPs also offer a consultancy service to ensure that operations are in-line with all relevant EU directives and other necessary regulations.
Our dedicated team of specialists will be happy to discuss our Clinical QP Services with you. Contact us on +1 779-208-1819 (US) or +44 1495 711 222 (UK/EU) or email firstname.lastname@example.org
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We deliver best-in-class clinical trial services with an unmatched reputation for flexibility, a client-centric experience, and a consultative approach. We provide a seamless service, including pharmaceutical development, clinical manufacturing, labeling, storage, and distribution.
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