Quality & QP Services

A quality-first approach to clinical trial supply

Our team is committed to maintaining high global standards of quality across our organization from clinical trial supply chain management to distribution. In addition to regular regulatory audits of our facilities, where applicable, in support of our licenses we also are subject to regular QA audits by our clients. At RxSource, product quality and patient safety are our top priority and are achieved through structured quality systems, procedures, and processes. Our QP services include auditing, batch review, and certification to support clinical trial sponsors with EU importation and batch release requirements.

Our goal is to surpass client and regulatory expectations while continuously improving quality in all we do, with a focus on improving patient lives by delivering medicines quickly and with the highest level of care and attention.

We are licensed by the following regulatory bodies:

• Canada - Health Canada, Drug Establishment License (DEL)
• USA - NJ Department of Health, Wholesale Distributor License (WDL)
• Europe – HPRA (Ireland) Investigational Medicinal Product Manufacturer/Importer

Authorisation (MIA) and Wholesaler Dealer’s License (WDL)