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.
Pubblicata da IEC e CEI l'Ed. 1.0 della Specifica tecnica per gli Equipaggiamenti elettrici di macchine utensili non portatili: IEC TS ...
ID 17685 | 26.09.2022 / In allegato Nota completa
UNI EN 1186-X - Norme della serie materie plastiche MOCA, nel dettaglio:
- UNI EN 1186-1:2003 Ma...
ID 24435 | 16.08.2025 / Preview attached
IEC 61496-3:2025
Safety of machinery - Electro-sensitive protective equipment - Part 3: Particular requirements for ...
Testata editoriale iscritta al n. 22/2024 del registro periodici della cancelleria del Tribunale di Perugia in data 19.11.2024