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bn:01631591n
Noun Concept
NL
No term available
EN
Under European Union law, the qualified person is responsible for certifying that each batch of a medicinal product meets all required provisions when released from a manufacturing facility within the EU, or imported into the EU. Wikipedia
English:
European Union
Relations
Sources
IS A
beroep
functie
FIELD OF THIS OCCUPATION
Good manufacturing practice
MAIN REGULATORY TEXT
EN
Medicinal Products Act

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