文献
J-GLOBAL ID:202102289416181166
整理番号:21A0280062
CIS諸国における医薬品製品の規制要求と登録プロセスの包括的レビュー【JST・京大機械翻訳】
A Comprehensive Review of Regulatory Requirements and Registration Process of Pharmaceutical Drug Products in CIS Countries
著者 (5件):
Pihwal Kapil
( Department of Pharmaceutical Science, Chaudhary Bansi Lal University, Bhiwani, Haryana, India)
,
Pawar Neelam
( Department of Pharmaceutical Science, Chaudhary Bansi Lal University, Bhiwani, Haryana, India)
,
Aamir Sheikh
( Department of Drug Regulatory & Export, Meher Pharma International, Sector 24, Rohini, New Delhi, India)
,
Alam Mohammad Shahbaz
( Department of Drug Regulatory & Export, Meher Pharma International, Sector 24, Rohini, New Delhi, India)
,
Rathee Vikas
( Department of Drug Regulatory & Export, Meher Pharma International, Sector 24, Rohini, New Delhi, India)
資料名:
Applied Clinical Research, Clinical Trials and Regulatory Affairs
(Applied Clinical Research, Clinical Trials and Regulatory Affairs)
巻:
7
号:
3
ページ:
162-176
発行年:
2020年
JST資料番号:
W3553A
ISSN:
2213-476X
資料種別:
逐次刊行物 (A)
記事区分:
文献レビュー
発行国:
不明 (ARE)
言語:
英語 (EN)