Law of December 19, 2014, on amending the Law - Pharmaceutical Law and certain other laws

Texts

The consolidated text (tekst ujednolicony) is unofficial; only the signed PDFs from Dziennik Ustaw / Monitor Polski are legally authentic.

Keywords

Related acts

Acts referring to this act

• Amending Acts: Law of 29 July 2005 on Counteracting Drug Addiction
• Amending Acts: Law of September 6, 2001, Pharmaceutical Law.
• Amending Acts: Law of October 28, 2002, on the liability of collective entities for offenses punishable by law.
• Amended Acts: Law of 7 June 2018 on amending the Law - Pharmaceutical Law and certain other laws
• Repeals Resulting From: 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
• Repeals Resulting From: Regulation of the Minister of Health of March 28, 2012 amending the regulation on Good Manufacturing Practice requirements
• Repeals Resulting From: Regulation of the Minister of Health of January 12, 2011, on the form of the manufacturing authorization for a medicinal product and an investigational medicinal product, and the form of the import authorization for a medicinal product and an investigational medicinal product
• Repeals Resulting From: Regulation of the Minister of Health of January 12, 2011, on the form of the application for an amendment to the manufacturing authorization for a medicinal product and an investigational medicinal product, and the form of the application for an amendment to the import authorization for a medicinal product and an investigational medicinal product
• Repeals Resulting From: 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
• Repeals Resulting From: Regulation of the Minister of Health of December 23, 2010, amending the regulation on Good Manufacturing Practice requirements
• Repeals Resulting From: Regulation of the Minister of Health of 24 February 2010 on the amount and method of covering costs related to inspections conducted by inspectors for manufacturing of the Chief Pharmaceutical Inspectorate
• Repeals Resulting From: Regulation of the Minister of Health of August 17, 2009, amending the regulation on Good Manufacturing Practice requirements
• Repeals Resulting From: Regulation of the Minister of Health of 1 October 2008 on Good Manufacturing Practice requirements
• Repeals Resulting From: Regulation of the Minister of Health of March 14, 2008 on the conditions for mail-order sale of medicinal products available without a prescription
• Repeals Resulting From: Regulation of the Minister of Health of 21 September 2007 on the register of manufacturers of active substances used in the production of veterinary medicinal products with anabolic, anti-infective, antiparasitic, hormonal or psychotropic properties
• Repeals Resulting From: Regulation of the Minister of Health of June 29, 2007 amending the regulation on the requirements that a qualified person responsible for the quality and batch control of a medicinal product before its market release should meet
• Repeals Resulting From: Regulation of the Minister of Health of March 10, 2006 on the amount and method of collecting fees for granting and changing permits for the manufacture of medicinal products and for granting and changing permits for the import of medicinal products
• Repeals Resulting From: Regulation of the Minister of Health of February 2, 2006 on the requirements that a qualified person responsible for the quality and batch control of a medicinal product before its market release should meet
• Repeals Resulting From: 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
• Repeals Resulting From: Regulation of the Minister of Health of 20 February 2003 on the transfer of data concerning the volume of trade in medicinal products by pharmaceutical wholesalers
• Repeals Resulting From: Regulation of the Minister of Health of July 10, 2013, amending the regulation on Good Manufacturing Practice requirements
• Repeals Resulting From: Regulation of the Minister of Health of July 26, 2002, on Good Distribution Practice procedures.
• Repeals Resulting From: 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