Home / Dz.U. 2008 nr 184 poz. 1143
Regulation of the Minister of Health of 1 October 2008 on Good Manufacturing Practice requirements
Rozporządzenie Ministra Zdrowia z dnia 1 października 2008 r. w sprawie wymagań Dobrej Praktyki Wytwarzania
Type
Regulation (Rozporządzenie)
Status
declared repealed (uznany za uchylony)
Announced
2008-10-01
Entry into force
2008-11-01
Texts
Keywords
Pharmaceutical MeansMedicines and Sanitary Articlesproduction
Related acts
Repealed Acts (1)
Amending Acts (4)
- Regulation of the Minister of Health of August 17, 2009, amending the regulation on Good Manufacturing Practice requirements · 2009-08-25
- Regulation of the Minister of Health of December 23, 2010, amending the regulation on Good Manufacturing Practice requirements · 2011-02-11
- Regulation of the Minister of Health of March 28, 2012 amending the regulation on Good Manufacturing Practice requirements · 2012-04-20
- Regulation of the Minister of Health of July 10, 2013, amending the regulation on Good Manufacturing Practice requirements · 2013-09-05
Information on Consolidated Text (1)
Legal Basis (1)
Legal Basis from Art. (1)
- Law of September 6, 2001, Pharmaceutical Law. · art. 39 ust. 4 pkt 1
Repeals Resulting From (1)
Acts referring to this act
- Repealing Acts: Regulation of the Minister of Health of October 2, 2006, on Good Manufacturing Practice requirements
- Acts Declared Repealed: Law of December 19, 2014, on amending the Law - Pharmaceutical Law and certain other laws
- Implementing Regulations: Law of September 6, 2001, Pharmaceutical Law.
- Amended Acts: Regulation of the Minister of Health of July 10, 2013, amending the regulation on Good Manufacturing Practice requirements
- Amended Acts: Regulation of the Minister of Health of March 28, 2012 amending the regulation on Good Manufacturing Practice requirements
- Amended Acts: Regulation of the Minister of Health of December 23, 2010, amending the regulation on Good Manufacturing Practice requirements
- Amended Acts: Regulation of the Minister of Health of August 17, 2009, amending the regulation on Good Manufacturing Practice requirements
- References: Regulation of the Minister of Health of 4 November 2008 on the forms of documents submitted in connection with a clinical trial of a medicinal product and on the amount and method of paying fees for commencing a clinical trial
- References: Regulation of the Minister of Health of March 28, 2012 amending the regulation on the form of the application for a manufacturing authorization for medicinal products and investigational medicinal products and the form of the application for an import authorization for medicinal products and investigational medicinal products
- Consolidated Text for an Act: Announcement of the Minister of Health of October 17, 2013, on the announcement of the consolidated text of the Regulation of the Minister of Health on Good Manufacturing Practice requirements