fda glp certification

完美工坊(統編:72673624)

吳靜美經營完美工坊已有2年5個月,統一編號:72673624在2017-09-20成立於新北市樹林區龍興街53號1樓販賣清潔用品製造業|化粧品製造業|食品什貨、飲料零售業|布疋、衣著、鞋、帽、傘、服飾品零售業...等商品·技術·服務詳細工商資訊完整紀錄。

保生西藥房(統編:60568909)

吳王木桂經營保生西藥房已有53年1個月,統一編號:60568909在1966-03-02成立於彰化縣大城鄉東城村中平路67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。

鳳仁藥局(統編:85879556)

陳茂盛　　　經營鳳仁藥局已有38年3個月,統一編號:85879556在1981-07-15成立於高雄市鳳山區北門里鳳仁路一街一 巷9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。

嵐田美容坊(統編:47414017)

柯榆婷經營嵐田美容坊已有3年2個月,統一編號:47414017在2016-06-22成立於臺中市豐原區陽明里府前街85號1樓販賣美容美髮服務業|無店面零售業|未分類其他服務業|布疋、衣著、鞋、帽、傘、服飾品零售業...等商品·技術·服務詳細工商資訊完整紀錄。

沐欣企業社(統編:47471261)

劉幗英經營沐欣企業社已有3年2個月,統一編號:47471261在2016-02-25成立於臺中市北屯區瀋陽路三段255號1樓販賣日常用品零售業|清潔用品零售業|化學原料零售業|化粧品零售業...等商品·技術·服務詳細工商資訊完整紀錄。

絲柔專業護膚(統編:78018596)

徐美琴經營絲柔專業護膚已有25年5個月,統一編號:78018596在1994-09-23成立於新竹縣新豐鄉員山村建興路一段144號販賣化粧品零售業|藥物、化粧品零售業...等商品·技術·服務詳細工商資訊完整紀錄。

緣緣美容工作坊(統編:99764350)

翁莉敏經營緣緣美容工作坊已有15年2個月,統一編號:99764350在2004-06-17成立於新北市中和區景平路722之3號2樓（現場僅供辦公室使用）販賣化粧品零售業|藥物、化粧品零售業...等商品·技術·服務詳細工商資訊完整紀錄。

健元藥局(統編:82079118)

黃東亮經營健元藥局已有39年1個月,統一編號:82079118在1980-05-09成立於高雄市鼓山區龍井里鼓山三路29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。

保壽藥房(統編:31194902)

周張月琴經營保壽藥房已有22年1個月,統一編號:31194902在1997-03-21成立於臺北市北投區石牌路一段166巷101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。

萬福堂藥局(統編:47075924)

何瑞銘經營萬福堂藥局已有39年1個月,統一編號:47075924在1980-03-13成立於新竹縣橫山鄉新興村9讚頭74號販賣西藥製造業|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。

fda glp certification·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

  • GLP Guidance Text - FDA

    www.fda.gov

    28 Aug 2013 ... Laboratory Practice (GLP) regulations for nonclinical laboratory studies conducted to support research and marketing applications for medical devices. FDA's guidance documents, including this guidance, do not establish legally enf

  • 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

  • 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

  • Online Training for ISO 9001, ISO 14001, ISO 13485, AS9100D, GMP, GLP, HACCP:

    www.caliso9000.com

    Online Training for ISO 9001, ISO 14001, ISO 13485, AS9100D, GMP, GLP, HACCP: SAE International, offers the CALISO courses, the best and most popular training program for ISO standards and FDA regulations. With over 30,000 courses and certificates ...

  • Guidance for Clinical Investigators, Sponsors, and IRBs

    www.fda.gov

    Contains Nonbinding Recommendations Guidance for Clinical Investigators, Sponsors, and IRBs1 Adverse Event Reporting to IRBs — Improving Human Subject Protection This guidance represents the Food and Drug Administration's (FDA's) current thinking on ...