handdesinfecterend fda-verordening

  • Huis
  • /
  • handdesinfecterend fda-verordening

handdesinfecterend fda-verordening

REGULATION (EU) 2017/ 745 OF THE EUROPEAN PARLIAMENT AND ...- handdesinfecterend fda-verordening ,(11) Union legislation, in par ticular Regulation (EC) No 1394/2007 of the European Parliament and of the Council (1) and Directive 2004/23/EC of the European Parliament and of the Council (2), is incomplete in respect of cer tain products manufactured utilising der ivatives of tissues or cells of human or igin that are non-viable or are renderedPCQI certificerende training | NormecFoodcareExporteer je naar de VS? Met de PCQI certificerende training van Training & Education word je in 2,5 dag PCQI gecertificeerd.



EUR-Lex - 32011R1169 - EN - EUR-Lex

(4) According to Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (3) it is a general principle of food law to provide a basis for consumers to make informed choices in relation to food ...

20 jaar 21 CFR Part 11: Electronische Gegevensbestanden ...

20 jaar geleden werd 21CFR part 11 Electronic records, Electronic Signatures gepubliceerd. 21 CFR Part 11 is een sectie in de Code of Federal Regulations (CFR), waarin de Amerikaanse Food and Drug Administration (FDA) wettelijke eisen met betrekking tot het gebruik van elektronische registraties en elektronische handtekeningen vastlegt. Part 11 werd ontwikkeld op verzoek van…

20 jaar 21 CFR Part 11: Electronische Gegevensbestanden ...

20 jaar geleden werd 21CFR part 11 Electronic records, Electronic Signatures gepubliceerd. 21 CFR Part 11 is een sectie in de Code of Federal Regulations (CFR), waarin de Amerikaanse Food and Drug Administration (FDA) wettelijke eisen met betrekking tot het gebruik van elektronische registraties en elektronische handtekeningen vastlegt. Part 11 werd ontwikkeld op verzoek van…

PCQI certificerende training | NormecFoodcare

Exporteer je naar de VS? Met de PCQI certificerende training van Training & Education word je in 2,5 dag PCQI gecertificeerd.

Quality System (QS) Regulation/Medical Device Good ...

Good Manufacturing Practices (GMP) / Quality Systems (QS) Regulation. Flexibility of the QS Regulation. The QS regulation embraces the same "umbrella'' approach to the CGMP regulation that was the ...

EUR-Lex - 32017R0745 - EN - EUR-Lex

(5) To the extent possible, guidance developed for medical devices at international level, in particular in the context of the Global Harmonization Task Force (GHTF) and its follow-up initiative, the International Medical Devices Regulators Forum (IMDRF), should be taken into account to promote the global convergence of regulations which contributes to a high level of safety protection ...

PCQI certificerende training | NormecFoodcare

Exporteer je naar de VS? Met de PCQI certificerende training van Training & Education word je in 2,5 dag PCQI gecertificeerd.

EUR-Lex - 32017R0746 - EN - EUR-Lex

(2) This Regulation aims to ensure the smooth functioning of the internal market as regards in vitro diagnostic medical devices, taking as a base a high level of protection of health for patients and users, and taking into account the small and medium-sized enterprises that are active in this sector. At the same time, this Regulation sets high standards of quality and safety for in vitro ...

20 jaar 21 CFR Part 11: Electronische Gegevensbestanden ...

20 jaar geleden werd 21CFR part 11 Electronic records, Electronic Signatures gepubliceerd. 21 CFR Part 11 is een sectie in de Code of Federal Regulations (CFR), waarin de Amerikaanse Food and Drug Administration (FDA) wettelijke eisen met betrekking tot het gebruik van elektronische registraties en elektronische handtekeningen vastlegt. Part 11 werd ontwikkeld op verzoek van…

Guidance on CLP - ECHA

The list below contains all the Guidance Documents which are available, or will be available, on this website. These documents have been developed with the participation of many stakeholders: Industry, Member States and NGOs.

EUR-Lex - 32017R0746 - EN - EUR-Lex

(2) This Regulation aims to ensure the smooth functioning of the internal market as regards in vitro diagnostic medical devices, taking as a base a high level of protection of health for patients and users, and taking into account the small and medium-sized enterprises that are active in this sector. At the same time, this Regulation sets high standards of quality and safety for in vitro ...

PCQI certificerende training | NormecFoodcare

Exporteer je naar de VS? Met de PCQI certificerende training van Training & Education word je in 2,5 dag PCQI gecertificeerd.

EUR-Lex - 32011R1169 - EN - EUR-Lex

(4) According to Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (3) it is a general principle of food law to provide a basis for consumers to make informed choices in relation to food ...

Quality System (QS) Regulation/Medical Device Good ...

Good Manufacturing Practices (GMP) / Quality Systems (QS) Regulation. Flexibility of the QS Regulation. The QS regulation embraces the same "umbrella'' approach to the CGMP regulation that was the ...

EUR-Lex - 32017R0746 - EN - EUR-Lex

(2) This Regulation aims to ensure the smooth functioning of the internal market as regards in vitro diagnostic medical devices, taking as a base a high level of protection of health for patients and users, and taking into account the small and medium-sized enterprises that are active in this sector. At the same time, this Regulation sets high standards of quality and safety for in vitro ...

EUR-Lex - 32017R0745 - EN - EUR-Lex

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance.

Dual-use trade controls - Trade - European Commission

Dual-use items are goods, software and technology that can be used for both civilian and military applications. The EU controls the export, transit and brokering of dual-use items so the EU can contribute to international peace and security and prevent the proliferation of Weapons of Mass Destruction (WMD).

EUR-Lex - 32004R1935 - EN - EUR-Lex

(1) Council Directive 89/109/EEC of 21 December 1988 on the approximation of the laws of the Member States relating to materials and articles intended to come into contact with foodstuffs (3) established general principles for eliminating the differences between the laws of the Member States as regards those materials and articles and provided for the adoption of implementing directives ...

Dual-use trade controls - Trade - European Commission

Dual-use items are goods, software and technology that can be used for both civilian and military applications. The EU controls the export, transit and brokering of dual-use items so the EU can contribute to international peace and security and prevent the proliferation of Weapons of Mass Destruction (WMD).

REGULATION (EU) 2017/ 745 OF THE EUROPEAN PARLIAMENT AND ...

(11) Union legislation, in par ticular Regulation (EC) No 1394/2007 of the European Parliament and of the Council (1) and Directive 2004/23/EC of the European Parliament and of the Council (2), is incomplete in respect of cer tain products manufactured utilising der ivatives of tissues or cells of human or igin that are non-viable or are rendered

Dual-use trade controls - Trade - European Commission

Dual-use items are goods, software and technology that can be used for both civilian and military applications. The EU controls the export, transit and brokering of dual-use items so the EU can contribute to international peace and security and prevent the proliferation of Weapons of Mass Destruction (WMD).

REGULATION (EU) 2017/ 745 OF THE EUROPEAN PARLIAMENT AND ...

(11) Union legislation, in par ticular Regulation (EC) No 1394/2007 of the European Parliament and of the Council (1) and Directive 2004/23/EC of the European Parliament and of the Council (2), is incomplete in respect of cer tain products manufactured utilising der ivatives of tissues or cells of human or igin that are non-viable or are rendered

EUR-Lex - 32011R1169 - EN - EUR-Lex

(4) According to Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (3) it is a general principle of food law to provide a basis for consumers to make informed choices in relation to food ...

EUR-Lex - 32004R1935 - EN - EUR-Lex

(1) Council Directive 89/109/EEC of 21 December 1988 on the approximation of the laws of the Member States relating to materials and articles intended to come into contact with foodstuffs (3) established general principles for eliminating the differences between the laws of the Member States as regards those materials and articles and provided for the adoption of implementing directives ...