UNI EN ISO 22716:2008
La norma fornisce le linee guida per la produzione, il controllo, l'immagazzinamento e la spedizione dei prodotti cosmetici.
Le Norme di Buona Fabbricazione (GMP), corrispondono a quella parte della assicurazione di qualità che ha lo scopo di assicurare che i prodotti vengano fabbricati in modo da risultare consistentemente di qualità adeguata per l’uso che se ne intende fare. Esse, pertanto, hanno per oggetto sia la produzione che il controllo di qualità.
The body of European Union legislation in the pharmaceutical sector is compiled in Volume 1 and Volume 5 of the publication "The rules governing medicinal products in the European Union":
- Volume 1 - EU pharmaceutical legislation for medicinal products for human use
- Volume 5 - EU pharmaceutical legislation for medicinal products for veterinary use
The basic legislation is supported by a series of guidelines that are also published in the following volumes of "The rules governing medicinal products in the European Union":
- Volume 2 - Notice to applicants and regulatory guidelines for medicinal products for human use
- Volume 3 - Scientific guidelines for medicinal products for human use
- Volume 4 - Guidelines for good manufacturing practices for medicinal products for human and veterinary use
- Volume 6 - Notice to applicants and regulatory guidelines for medicinal products for veterinary use
- Volume 7 - Scientific guidelines for medicinal products for veterinary use
- Volume 8 - Maximum residue limits
- Volume 9 - Guidelines for pharmacovigilance for medicinal products for human and veterinary use
- Volume 10 - Guidelines for clinical trial
Medicinal products for paediatric use, orphans, herbal medicinal products and advanced therapies are governed by specific rules.