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AP Consulting: Medical Devices
http://www.fdaapc.com/medical_devices.htm
AP Consulting: Contact Us. AP Consulting is a regulatory consulting firm that specializes in FDA issues pertaining to medical devices and dietary supplements. As a former Investigator’s Performance Auditor. For FDA, I can help you to prepare for an FDA inspection. Hire someone who used to do it as a professional career. We are available to travel to most countries around the globe. Contact AP Consulting Today. We offer the following assistance to medical device manufacturers:. Assist with import issues.
AP Consulting: About The Consultant
http://www.fdaapc.com/about_the_consultant.htm
AP Consulting: Contact Us. AP Consulting is a regulatory consulting firm that specializes in FDA issues pertaining to medical devices and dietary supplements. As a former Investigator’s Performance Auditor. For FDA, I can help you to prepare for an FDA inspection. Hire someone who used to do it as a professional career. We are available to travel to most countries around the globe. Contact AP Consulting Today. FDA/ORA Supervisory Investigator and Medical Device Supervisor.
AP Consulting: Home
http://www.fdaapc.com/default.htm
AP Consulting: Contact Us. AP Consulting is a regulatory consulting firm that specializes in FDA issues pertaining to medical devices and dietary supplements. As a former Investigator’s Performance Auditor. For FDA, I can help you to prepare for an FDA inspection. Hire someone who used to do it as a professional career. We are available to travel to most countries around the globe. Contact AP Consulting Today.
AP Consulting: Dietary Supplements
http://www.fdaapc.com/dietary_supplements.htm
AP Consulting: Contact Us. AP Consulting is a regulatory consulting firm that specializes in FDA issues pertaining to medical devices and dietary supplements. As a former Investigator’s Performance Auditor. For FDA, I can help you to prepare for an FDA inspection. Hire someone who used to do it as a professional career. We are available to travel to most countries around the globe. Contact AP Consulting Today. We offer the following assistance to medical device manufacturers:. The Bioterrorism Act of 2002.
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Fudan University Alumni Association of Northern California. January 14, 2017. 亲爱的校友们，上海的朋友们， 一年一度的 上海之夜 上海九大高校校友联欢即将于2017年2月18日晚在Palo Alto Sofia University的大礼堂盛大登场。 August 1, 2016. 时间 (When) 2016年8月27日 (August 27, 2016), 周六 (Saturday), 10:00 AM 14:00 PM 地点 (Where) Rengstorff Park 201 South Rengstorff Ave, Mountain View, CA 94040 欢迎 所有的上海高校校友及亲朋好友 欢迎大家网上报名注册。 Online 成人网上票价$12, 儿童12岁以下网上票价$5. Walk in 成人 $15, 儿童12岁以下 $8. 报名链接如下: for adult for child 特别鸣谢各位赞助活动的热心校友们，他们是 …. February 3, 2016. October 15, 2015.
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AP Consulting: Contact Us. AP Consulting is a regulatory consulting firm that specializes in FDA issues pertaining to medical devices and dietary supplements. As a former Investigator’s Performance Auditor. For FDA, I can help you to prepare for an FDA inspection. Hire someone who used to do it as a professional career. We are available to travel to most countries around the globe. Contact AP Consulting Today.
FDA Apostille | Apostille FDA
As of March 1, 2014, the United States Food and Drug Administration (FDA). For Devices and Radiological Health (CDRH) will no longer notarize FDA CDRH export certificates. Certificates to Foreign Government, Certificates of Exportability and Non-Clinical Research Use Only Certificates will still be issued by the FDA, but notary services will no longer be provided. US Department of State Office of Authentications Walk In Service Address:. US Department of State. Washington, DC 20006. Along with a written ...
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協助美國FDA查廠, 2014至今, 零缺失的廠商: 美迪, 茂晶(血糖儀), 塘廈亞弘電, 譜安, 中山康利寶, 申一. 專業輔導 ISO 9001, ISO 13485, ISO 14971, ISO 22716, GMP, CE 標示, FDA 510k. 與 化妝品FDA註冊, GMP ISO 22716. 美國 中小企業 資格, 可享有 FDA510k 審核費50. 協助廠商建立正確的 : 品質管理系統( ISO 9001, ISO13485: 醫療器材(MD). GMP, TQM, MRP ), 化妝品GMP. 以及申請 : 加拿大 CMDCAS. 標示 與 美國 FDA 510k. 中歐學會是由內政部管理的全國性社會團體, 以提升國內廠商品質管理系統, 協助申請歐聯CE標示與美國FDA ; 為美國FDA正式登錄的顧問機構. 中歐學會的輔導經驗豐富, 自 1999. 年成立以來, 主要實績 : (參閱. 家廠商 申請2018年度 FDA 註冊與列名. 5 2001 2002年經濟部補助醫療器材GMP輔導案每年15家廠商, 其中每年各有 9.
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Chesapeake Regulatory Group, Inc.
Content on this page requires a newer version of Adobe Flash Player. Each of us at CRG has over 30 years of experience helping companies get their products approved by the FDA. Let us put our experience to work for you.". Working closely with our clients for over 20 years. Contact us today for more information on how CRG can help you achieve success. Chesapeake Regulatory Group, Inc. 2012.
