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- L-AĦĦAR AĠĠORNAMENTI
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Tip:
Subsidiary Legislation
Short Title: Good Clinical Practice and Requirements for Manufacturing or Import Authorisation of Investigational Medicial Products (Human Use) Regulations
Titolu:
Good Clinical Practice and Requirements for Manufacturing or Import Authorisation of Investigational Medicial Products (Human Use) Regulations
Link tal-ELI:
eli/sl/458.47
Point in Time:
01/01/2022
Keywords
:
Human use, Good Clinical Practice, Manufacturing or Import Authorisation, Investigational Medicial Products
Language:
Ingliż
Malti
Format:
PDF