PNR Pharma

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PNR Pharma offers Qualified Person (QP) and importation services to the European Union and United Kingdom, for both commercial and clinical trial products, including site audits, QP declarations and QP certification for traditional and ATMP products. Importation and depot management, QP consultancy, QA and Project Management activities. PNR Pharma can manage your project throughout its lifecycle with direct access to your designated Project Manager and Qualified Person. To ensure you have a QP available at all times, you will have a primary project QP and a designated deputy QP to ensure your project is always supported.

PNR Pharma offers EU and UK QP batch certification for Commercial and IMP Products via licences issued by the HPRA and MHRA..

Through our latest GMP certified warehouse in the UK we can provide comprehensive support services to clinical trials including warehousing, temperature controlled storage & distribution, secondary packaging and labelling and project management.

Members of the PNR Pharma Consulting Ltd team have been deemed eligible to act as Compliance Monitors as part of the MHRA pilot programme.

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audits, qp services, remediation projects, clinical trials, mia for imp, mia for commercial products, batch release, qp declaration, storage & distribution project management, qp consultancy, secondary packaging, comparators sourcing, auxiliary medicines, imdp review, qp certification biologics, gene therapy, vaccines & traditional dosage forms, audit preparation, training

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