Home / Dz.U. 2011 nr 20 poz. 109
Regulation of the Minister of Health of January 12, 2011, 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
Rozporządzenie Ministra Zdrowia z dnia 12 stycznia 2011 r. w sprawie wzoru wniosku o wydanie zezwolenia na wytwarzanie produktów leczniczych i badanych produktów leczniczych oraz wzoru wniosku o wydanie zezwolenia na import produktów leczniczych i badanych produktów leczniczych
Type
Regulation (Rozporządzenie)
Status
declared repealed (uznany za uchylony)
Announced
2011-01-12
Entry into force
2011-02-12
Texts
Keywords
Pharmaceutical MeansMedical ProductsimportpermitsMedicines and Sanitary Articlesproduction
Related acts
Legal Basis (1)
Legal Basis from Art. (1)
- Law of September 6, 2001, Pharmaceutical Law. · art. 39 ust. 4 pkt 3
Repeals Resulting From (1)
Acts referring to this act
- Acts Declared Repealed: Law of December 19, 2014, on amending the Law - Pharmaceutical Law and certain other laws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 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 April 18, 2013, on the promulgation of the consolidated text of the Regulation of the Minister of Health on the form of the application for a permit to manufacture medicinal products and investigational medicinal products, and the form of the application for a permit to import medicinal products and investigational medicinal products