fda glp list

龍佳西藥房(統編:81855694)

黃俊龍經營龍佳西藥房已有26年6個月,統一編號:81855694在1993-10-21成立於高雄市前鎮區瑞隆路321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。

正大藥房(統編:66342133)

吳清松經營正大藥房已有43年8個月,統一編號:66342133在1976-12-08成立於嘉義縣6腳鄉崙陽村崙仔132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。

隆發西藥行(統編:02195157)

陳恭宗經營隆發西藥行已有30年,統一編號:02195157在1989-04-18成立於新北市泰山區明志路二段31號1樓販賣西藥製造業|西藥批發業|農產品零售業...等商品·技術·服務詳細工商資訊完整紀錄。

義達西藥房(統編:11795408)

林王天珠經營義達西藥房已有52年8個月,統一編號:11795408在1967-12-28成立於臺北市中山區北安路575號1樓販賣西藥製造業|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。

仁富藥房(統編:60442326)

陳仁甫經營仁富藥房已有48年8個月,統一編號:60442326在1971-12-03成立於彰化縣北斗鎮新政里中華路231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。

西河藥房(統編:98072581)

李正平經營西河藥房已有25年3個月,統一編號:98072581在1994-01-05成立於宜蘭縣羅東鎮竹林里復興街127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。

九福鐘錶眼鏡行(統編:88864851)

陳俊宏經營九福鐘錶眼鏡行已有24年7個月,統一編號:88864851在1995-11-03成立於高雄市鼓山區忠正里九如四路943號販賣西藥製造業|西藥批發業|鐘錶批發業...等商品·技術·服務詳細工商資訊完整紀錄。

光明西藥房(統編:66817840)

張立興經營光明西藥房已有29年2個月,統一編號:66817840在1990-02-20成立於苗栗縣卓蘭鎮中街里中街里民生路13號販賣西藥製造業|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。

錦燁西藥房(統編:81674390)

蕭銘章經營錦燁西藥房已有23年,統一編號:81674390在1996-04-25成立於臺北市信義區忠孝東路五段790巷84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。

馬偕藥局(統編:02263696)

孔巧佳經營馬偕藥局已有28年3個月,統一編號:02263696在1991-01-07成立於新北市淡水區民生路?76號?0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。

fda glp list·相關網站分享資訊

  • Nonclinical Laboratories Inspected under Good Laboratory Practices

    www.fda.gov

    The FDA conducts careful inspections of facilities that perform nonclinical laboratory studies to determine compliance with Part 58 (Good Laboratory Practice for Nonclinical Laboratory Studies) of Title 21 of the Code of Federal Regulations. Nonc

  • Good Laboratory Practice Regulations - FDA

    www.fda.gov

    18 May 2015 ... Good Laboratory Practice Regulations. [Docket No. 83N-0142]. 52 FR 33768. September 4, 1987. ACTION: Final rule. SUMMARY: The Food and Drug Administration (FDA) is issuing a final rule that amends the regulations that specify good

  • Good Laboratory Practice Regulations - FDA

    www.fda.gov

    18 May 2015 ... Since June 20, 1979, the agency has been asked many questions on the Good Laboratory Practice regulations (GLPs, 21 CFR 58). In accord with agency procedures, responses have been prepared and copies of the associated correspondenc

  • Good Laboratory Practice Regulations Management Briefings ... - FDA

    www.fda.gov

    18 May 2015 ... ON THE GOOD LABORATORY PRACTICE REGULATIONS POST CONFERENCE REPORT. On May 1, 2 and 3, 1979, FDA conducted half-day briefing sessions in Washington, Chicago and San Francisco on the Good Laboratory Practice Regulations. The purpos

  • Good Laboratory Practices Questions and Answers

    www.fda.gov

    1981 GLP Questions & Answers GOOD LABORATORY PRACTICE QUESTIONS AND ANSWERS Since June 20, 1979, ... Will a laboratory subsequently be notified of GLP deviations not listed on the FDA-483? This does happen. The FDA investigator ...

  • CFR - Code of Federal Regulations Title 21

    www.accessdata.fda.gov

    This information is current as of April 1, 2017. This online reference for CFR Title 21 is updated once a year. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). This database includes a codification

  • GMP Publications - Official Site

    www.gmppublications.com

    Code of Federal Regulations Mini-Handbooks as provided by the Food and Drug Administration FDA. The laws for Pharmaceuticals, BioTechnology, Medical Device and Regulatory Industry. Quality Assurance QA, Blood, Biologics, Drug and Food Industry

  • GxP - Wikipedia

    en.wikipedia.org

    GxP is a general abbreviation for the "good practice" quality guidelines and regulations. The "x" stands for the various fields, including the pharmaceutical and food industries, for example good agricultural practice, or GAP. A "c" or "C" is sometimes ad

  • Warning Letters - FDA

    www.fda.gov

    Topics on this Page: Ways to View/Browse Warning Letters; More Information About Warning Letters Posted Here; Recently Posted Warning Letters ...

  • Clinical Investigator Inspection Search - Food and Drug Administration

    www.accessdata.fda.gov

    U.S. Food and Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993 1-888-INFO-FDA (1-888-463-6332) Contact FDA