active substance manufacturing / manufacturing operation / biological medicinal products / supply chain / active substance manufacturers / manufacturing activity / human and veterinary medicinal products / active substance manufacturing sites / manufacturing site i.e. / timely processing / manufacturing steps / medicinal product / chemical entities / veterinary medicinal products / pharmaceutical active substance / manufacturing site / manufacturing / immunological veterinary medicinal products / veterinary medicinal product / medicinal products / intermediate manufacturing / convergent drug substance manufacturing process / active substance manufacturer / /
Organization
EU GMP / European Medicines Agency / European Commission / EEA / European Union / European Parliament / E-mail info@ema.europa.eu Website www.ema.europa.eu An / / /
21 May 2014 EMA[removed]Compliance and Inspections Department Guidance for the template for the qualified person’s declaration concerning GMP compliance of active