WHO Guideline Submission of documentation for a multisource (generic) finished pharmaceutical product: quality part

Titel:
WHO Guideline Submission of documentation for a multisource (generic) finished pharmaceutical product: quality part
Kurztitel:
Annex 6, WHO Technical Report Series 986
Herkunft/Verlag:

WHO headquarters, Avenue Appia 20, 1211 Geneva 27, Switzerland, Telephone: (+ 41 22) 791 21 11, Facsimile (fax): (+ 41 22) 791 3111, Telex: 415 416, www.who.int

Dokumentenart:
Guideline
Inhalt:
Unterstützung für Antragsteller hinsichtlich der Struktur des Quality Parts des Zulassungsantrags

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