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Publikováno v:
International Journal of Drug Regulatory Affairs. 10:32-41
This review article helps to study the practical aspects of different phases of life cycle of pharmaceutical products including sterile and non-sterile dosage forms in regulated market of Europe, to study the European standards and their requirements
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8265c68a338d8ba572182af357b4f85f
https://doi.org/10.22270/ijdra.v10i3.551
https://doi.org/10.22270/ijdra.v10i3.551
