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.
