Marketing authorization of pharmaceutical products with special reference to multisource (generic) products
a manual for National Medicines Regulatory Authorities (NMRAs)
World Health Organization
creator
text
Geneva
WHO
2011
monographic
eng
148 page
Legislation, Drug
Pharmaceutical Preparations
Drugs, Generic
Handbook
9789241501453
https://apps.who.int/iris/bitstream/handle/10665/44576/9789241501453_eng.pdf?sequence=1&isAllowed=y
https://apps.who.int/iris/bitstream/handle/10665/44576/9789241501453_eng.pdf?sequence=1&isAllowed=y
201214
20201214095407.0
D0001B000047