fda glp guidance documents
蘇蔡秋蓮經營慶誠西藥房已有33年3個月,統一編號:01417379在1986-07-08成立於臺北市萬華區萬大路277巷3號1樓販賣西藥製造業|西藥批發業|化粧品色素販賣業...等商品·技術·服務詳細工商資訊完整紀錄。
陳慶麗經營致康西藥房已有39年4個月,統一編號:43798322在1980-08-06成立於桃園市桃園區青溪里中央街153號販賣西藥製造業|西藥批發業|西藥零售業...等商品·技術·服務詳細工商資訊完整紀錄。
盧之義經營南星藥局已有38年1個月,統一編號:43852676在1981-05-01成立於桃園市桃園區大林里桃鶯路311號販賣西藥製造業|西藥批發業|西藥零售業...等商品·技術·服務詳細工商資訊完整紀錄。
呂光泰經營三泰藥局已有37年8個月,統一編號:81213221在1982-12-29成立於高雄市苓雅區正心里建國一路116號販賣西藥製造業|西藥批發業|化粧品色素販賣業...等商品·技術·服務詳細工商資訊完整紀錄。
魏俊介經營鴻福西藥房已有35年1個月,統一編號:40661049在1984-03-07成立於宜蘭縣頭城鎮大溪里外大溪路308號販賣西藥製造業|西藥批發業|化粧品色素販賣業...等商品·技術·服務詳細工商資訊完整紀錄。
鄭惠壬經營安隆中西藥局已有28年1個月,統一編號:76856167在1991-03-01成立於新北市新莊區建褔路69巷31號1樓販賣西藥製造業|動物用藥品批發業|西藥批發業...等商品·技術·服務詳細工商資訊完整紀錄。
宋培安經營明曜藥局已有25年7個月,統一編號:77880432在1994-11-25成立於臺北市大安區忠孝東路四段170巷5弄18號1樓販賣西藥製造業|西藥批發業|化粧品色素販賣業...等商品·技術·服務詳細工商資訊完整紀錄。
葉彩美經營建成西藥房已有36年7個月,統一編號:59329070在1983-11-02成立於彰化縣和美鎮中寮里東興路13號販賣西藥製造業|西藥批發業|化粧品色素販賣業...等商品·技術·服務詳細工商資訊完整紀錄。
柯清山經營柯藥局已有42年3個月,統一編號:83023009在1977-07-01成立於高雄市楠梓區東寧里楠梓東街164號販賣西藥製造業|西藥批發業|化粧品色素販賣業...等商品·技術·服務詳細工商資訊完整紀錄。
王靜雄經營忠山西藥房已有42年8個月,統一編號:83628859在1977-12-19成立於高雄市左營區尾北里菜公路50號販賣西藥製造業|西藥批發業|化粧品色素販賣業...等商品·技術·服務詳細工商資訊完整紀錄。
fda glp guidance documents·相關網站分享資訊
• couv.Handbook/1à4 13.8.2001 23:26 Page 3
www.who.int
The Good Laboratory Practice (GLP) Handbook is designed to serve as an aid for those countries who wish to upgrade their laboratories to GLP status. It has been devel-oped as part of a significant and wide-ranging technology transfer and capacity building
Global Bioequivalence / Bioavailability Regulatory Guidance Documents §¯`·.¸¸.·´¯`·.¸¸.
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Guidelines & Guidance Documents ICH WHO EMA DKMA FDA HPFB PMDA MCC TGA Medsafe CDSCO DGDA PAHO ANVISA Secr. de Salud ANMAT INVIMA SFDA JFDA EDA ACCSQ BPFK FDA HSA NA-DFC KFDA CDE CFDA MHSD EEC Swissmedic
Search for FDA Guidance Documents > The Applicability of Good ...
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23 Jul 2015 ... The Applicability of Good Laboratory Practice in Premarket Device ... This
guidance document is being distributed for comment purposes only.
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26 Mar 2018 ... FDA's guidance documents, including this guidance, do not establish ..... (21 CFR
Part 820), and the Good Laboratory Practice for Nonclinical ...
Proposed Regulations and Draft Guidances - FDA
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L. 112-144), signed into law on July 9, 2012, amended section 520(m) of the
FD&C Act. This guidance document also reflects changes in the HDE program ...
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23 Mar 2018 ... FDA has developed this guidance document to assist industry in designing ...
You should follow Good Laboratory Practices (GLP) for all animal ...
Guidance for Industry - Part 11, Electronic Records; Electronic ... - FDA
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11) are referred to in this guidance document as predicate rules. ... Part 211), the
Quality System regulation (21 CFR Part 820), and the Good Laboratory Practice.
Guidance for Industry - Food and Drug Administration
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Contains Nonbinding Recommendations Guidance for Industry and Reviewers1 Exploratory IND Studies This guidance represents the Food and Drug Administration's (FDA's) current thinking on this topic. It does not create or confer any rights for or on any pers
Links to National Web Sites on Good Laboratory Practice - OECD
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Data and research on test guidelines including chemical testing and assessment, chemical safety, animal welfare, endocrine disrupters, good laboratory practice (GLP), Mutual Acceptance of Data (MAD)., OECD Member countries information regarding GLP on the
