Services from Contracted Responsible Person (RP), Qualified Person (QP), Person Responsible from Quality (PRQ)

Our team of Qualified Persons (QP) and Responsible Persons (RP) operate in line with strict EU GMP/GDP (Good Manufacturing Practice/ Good Distribution Practice) guidelines, only authorising the release of medicinal products for sale in EU markets after having ensured that such products are manufactured by National Competent Authority (NCA) GMP licensed companies and imported by NCA licensed traders and wholesalers.

Our company offers batch acceptance, batch releasing, and license maintenance services for these activities.

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More services:

EU Market Accession Contract Responsible Person (RP), Qualified Person (QP) provision EU GMP/GDP/GACP Audits and Licensing FMD Decommissioning of 2D Bar Codes Medical Devices Pharmacovigilance Laboratory Testing Contract Manufacturing Clinical Trials Logistics Consultation and Warehousing Food Supplements and Cosmetics Registration
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