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GMP
Results: 1048

#	Item
861	Dear Sir/Madam, Please find below the feedback from Sandoz on guidelines on the formalised RA for ascertaining the appropriate GMP for excipients of medicinal products for human use Best regards, Marc Leeflang Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-07 08:57:36 Technology assessment Risk management Evaluation Reliability engineering Risk assessment Risk Probability Impact assessment
862	Comments from the European Industrial Pharmacists Group on the Revised GMP Guidelines Chapters 3 and 5 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-07 09:04:05 Validation Validity Pharmaceutical industry Clinical research Quality
863	EAEPC contribution to the public consultation on the revision of EU GMP Annex 16: ‘Certification by a Qualified Person and Batch Release’ Brussels, 14th January 2014 General Comments Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-01-31 06:07:24 European Free Trade Association Parallel import Traceability International relations Technology Business EFTA Court Clinical research Qualified Person
864	BPIs Comments on GMP Draft Annex 16 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-28 04:09:47 Qualified Person Computing QP Software Pharmaceuticals policy Clinical research
865	30 April 2013 Submission of comments on Risk Assessment for GMP for Excipients Comments from: Name of organisation or individual Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-07 08:57:31 Ethics Actuarial science Project management Security Risk assessment Comment Systems engineering process Management Risk Risk management
866	Brussels, 29th April, 2013 Subject : Public consultation on the Draft Guidelines on the formalised risk assessment for ascertaining the appropriate GMP for excipients of medicinal products for human use Dear Sir/Madam, E Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-11-07 08:59:21 Pharmacology Food safety Good manufacturing practice CEFIC Excipient Research Health Business International Pharmaceutical Excipients Council Pharmaceutical industry Pharmaceuticals policy Clinical research
867	Report on Analysis of Results SEE-GREEN Grundtvig[removed]LLP[removed]IT-GRUNDTVIG-GMP Add to Reading List Source URL: www.see-green.eu Language: English - Date: 2014-02-20 09:14:56 Technology Energy development Sustainable building Bulgarian Energy Holding Energy conservation Energy audit Sustainable energy Maritsa Iztok Complex NEK EAD Energy Energy economics Energy policy
868	SEE-GREEN Grundtvig[removed]LLP[removed]IT-GRUNDTVIG-GMP SEE-GREEN: Report of Analysis Add to Reading List Source URL: www.see-green.eu Language: English - Date: 2014-02-18 17:26:26 Energy conservation Sustainable building Environment Environmental issues with energy Sustainable energy Energy service company Energy Energy economics Energy policy
869	第三篇科技活動與成就－應用研究與技術發展業及追蹤管理，並策劃使 GMP 認證商品優 Add to Reading List Source URL: 59.56.176.111 Language: Korean - Date: 2011-01-11 23:24:57
870	DELEGATED ACT ON THE PRINCIPLES AND GUIDELINES OF GMP FOR ACTIVE SUBSTANCES IN MEDICINAL PRODUCTS FOR HUMAN USE Response of the Czech Republic to the Concept Paper submitted for public consultation 1. Extension of the Di Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:53 Qualified Person EudraLex Directive Health Science Pharmaceuticals policy Clinical research Medicinal product

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