fda glp guidance documents

  • 六和西藥房 桃園市

    六和西藥房經由陳明興　　開業於桃園市中壢區中原里興農路149號已有33年2個月(1986-12-24),開立統編:45087430提供消費者西藥製造業|西藥批發業|西藥零售業各種商品·技術·服務。…

  • 信茂藥局 高雄市

    信茂藥局經由王惠君開業於高雄市苓雅區林西里廣州一街49號1樓已有23年2個月(1996-08-22),開立統編:06681806提供消費者西藥製造業|西藥批發業|化粧品色素販賣業各種商品·技術·服務。…

  • 永和堂藥局 彰化縣

    永和堂藥局經由黃瑞琳　開業於彰化縣伸港鄉新港村新港路233號已有19年1個月(2000-11-17),開立統編:98614100提供消費者西藥製造業|中藥製造業|中藥批發業各種商品·技術·服務。…

  • 泰佑藥局 宜蘭縣

    泰佑藥局經由林麗玲開業於宜蘭縣礁溪鄉大忠村礁溪路45號已有25年6個月(1994-04-18),開立統編:40526522提供消費者西藥製造業|西藥批發業|化粧品色素販賣業各種商品·技術·服務。…

  • 東京西藥房 高雄市

    東京西藥房經由李辰雄開業於高雄市三民區正興里建工路685號已有9年4個月(2010-06-11),開立統編:75276508提供消費者西藥製造業|西藥批發業|化粧品色素販賣業各種商品·技術·服務。…

  • 力安西藥房 臺南市

    力安西藥房經由周月英開業於臺南市歸仁區後市里中山路330號已有10年(2009-10-09),開立統編:06603443提供消費者西藥製造業|西藥批發業|西藥零售業各種商品·技術·服務。…

  • 利昌行 基隆市

    利昌行經由王德明開業於基隆市仁愛區南榮路3Ｏ9號已有8年5個月(2011-05-06),開立統編:00657033提供消費者西藥製造業|西藥批發業|化粧品色素販賣業各種商品·技術·服務。…

  • 泰安西藥房 高雄市

    泰安西藥房經由林英順開業於高雄市鹽埕區陸橋里富野路129號已有1年9個月(2018-01-22),開立統編:83421702提供消費者西藥製造業|西藥批發業|化粧品色素販賣業各種商品·技術·服務。…

  • 鴻生西藥房 新北市

    鴻生西藥房經由杜鴻章開業於新北市三峽區民生街4號1Ｆ已有30年4個月(1989-06-23),開立統編:34593024提供消費者西藥製造業|西藥批發業|化粧品色素販賣業各種商品·技術·服務。…

  • 進安西葯房 臺南市

    進安西葯房經由林吳嫦娥開業於臺南市北區大仁里旭日街11號1樓已有14年(2005-10-04),開立統編:78656502提供消費者西藥製造業|動物用藥品批發業|西藥批發業各種商品·技術·服務。…

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fda glp guidance documents·相關網站分享資訊

  • 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

  • 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

  • Part 58 (Good Laboratory Practice for Nonclinical Laboratory ... - FDA

    www.accessdata.fda.gov

    Subpart A--General Provisions · § 58.1 - Scope. § 58.3 - Definitions. § 58.10 - Applicability to studies performed under grants and contracts. § 58.15 - Inspection of a testing facility. Subpart B--Organization and Personnel · § 58.29

  • 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

  • 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 ...

  • Labcompliance - Validation and Compliance for FDA and Other Agencies

    www.labcompliance.com

    Labcompliance News May Focused stakeholder consultation for draft PIC/S Guidance on Data Integrity Pakistan Applies for PIC/S Pre-Accession FDA Warning Letter recommends restricting access to computer system, and always enabling audit trail function

  • Consultants - XFDA INVESTIGATORS

    www.xfdainvestigators.com

    Christopher Smith, Coastal Pharmaceutical Consultants, Inc. Chris is a Quality Assurance and Regulatory Affairs accredited (CQE and RAC) professional with more than 30 years combined FDA and Industry experience. His expertise expands across a wide area of

  • Good Laboratory Practice for Nonclinical Laboratory Studies - FDA

    www.fda.gov

    Current FDA regulations describing good laboratory practice (GLP) ...... Act,” June 2010. http://www.sba.gov/sites/default/files/rfaguide.pdf, accessed November 6 ...

  • handbook good laboratory practice (glp) - World Health Organization

    www.who.int

    1997年11月26日 - TDR developed a Good Laboratory Practices (GLP) series in 2001, ..... led to the FDA's publication of Proposed Regulations on GLP in 1976,.