Home / Dz.U. 2013 poz. 1245
Law of September 27, 2013, on the amendment of the law - Pharmaceutical Law and certain other laws
Ustawa z dnia 27 września 2013 r. o zmianie ustawy - Prawo farmaceutyczne oraz niektórych innych ustaw
Type
Law (Ustawa)
Status
in force (obowiązujący)
Announced
2013-09-27
Entry into force
2013-11-25
Texts
The consolidated text (tekst ujednolicony) is unofficial; only the signed PDFs from Dziennik Ustaw / Monitor Polski are legally authentic.
Keywords
research and certificationFeldshersDoctorsVeterinariansPharmacistsMedicines and Sanitary ArticlesPharmaceutical LawPharmaceutical MeanspatientsmidwivesDentistsregisterspharmaceutical chambersnursing
Related acts
Acts Declared Repealed (8)
- Regulation of the Minister of Health of December 28, 2012 amending the regulation on organizational units that conduct quality testing of medicinal products and veterinary medicinal products, and the fees charged for these tests · 2013-11-25
- Regulation of the Minister of Health of April 30, 2012, on making changes to the permit and documentation concerning the marketing of a medicinal product · 2013-11-25
- Regulation of the Minister of Health of March 23, 2011, on the form of applications for extension or shortening of the validity period of a marketing authorization for a medicinal product · 2013-11-25
- Regulation of the Minister of Health of April 2, 2010, on the method of submitting documentation attached to the application for marketing authorization of a medicinal product · 2013-11-25
- Regulation of the Minister of Health of 10 February 2010 on the form of an application for a marketing authorization for a medicinal product · 2013-11-25
- Regulation of the Minister of Health of July 6, 2004, on the form of the application for a permit for parallel import of a medicinal product and the detailed list of data and documents covered by the application for amendment of this permit · 2013-11-25
- Regulation of the Minister of Health of 30 May 2003 on the organisational units that conduct qualitative tests of medicinal products and veterinary medicinal products, and the fees charged for these tests · 2013-11-25
- Regulation of the Minister of Health of 17 February 2003 on the monitoring of medicinal product safety · 2013-11-25
Amended Acts (10)
- Law of 18 March 2011 on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products · 2013-11-25
- Law of 15 July 2011 on the professions of nurse and midwife · 2013-11-25
- Law of November 6, 2008, on Patient Rights and the Patient Ombudsman · 2013-11-25
- Law of 8 September 2006 on State Medical Rescue · 2013-11-25
- Law of October 28, 2002, on the liability of collective entities for offenses punishable by law. · 2013-11-25
- Law of September 6, 2001, Pharmaceutical Law. · 2013-11-25
- Law of July 27, 2001, on laboratory diagnostics. · 2013-11-25
- Law of 5 December 1996 on the professions of physician and dentist. · 2013-11-25
- Law of April 19, 1991, on Pharmaceutical Chambers. · 2013-11-25
- Law of 20 July 1950 on the profession of feldsher. · 2013-11-25
References (6)
- Law of 18 March 2011 on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
- Law of November 6, 2008, on Patient Rights and the Patient Ombudsman
- Law of December 5, 2008, on the prevention and combating of infections and infectious diseases in humans
- Law of 6 September 2001 on access to public information
- Law of 6 June 1997 - Penal Code
- Law of 16 April 1993 on combating unfair competition.
Acts referring to this act
- Amending Acts: Law of 15 July 2011 on the professions of nurse and midwife
- Amending Acts: Law of November 6, 2008, on Patient Rights and the Patient Ombudsman
- Amending Acts: Law of October 28, 2002, on the liability of collective entities for offenses punishable by law.
- Amending Acts: Law of September 6, 2001, Pharmaceutical Law.
- Amending Acts: Law of July 27, 2001, on laboratory diagnostics.
- Amending Acts: Law of 5 December 1996 on the professions of physician and dentist.
- Amending Acts: Law of April 19, 1991, on Pharmaceutical Chambers.
- Amending Acts: Law of 20 July 1950 on the profession of feldsher.
- Amending Acts: Law of 8 September 2006 on State Medical Rescue
- Amending Acts: Law of 18 March 2011 on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
- Repeals Resulting From: Regulation of the Minister of Health of July 6, 2004, on the form of the application for a permit for parallel import of a medicinal product and the detailed list of data and documents covered by the application for amendment of this permit
- Repeals Resulting From: Regulation of the Minister of Health of April 30, 2012, on making changes to the permit and documentation concerning the marketing of a medicinal product
- Repeals Resulting From: Regulation of the Minister of Health of March 23, 2011, on the form of applications for extension or shortening of the validity period of a marketing authorization for a medicinal product
- Repeals Resulting From: Regulation of the Minister of Health of April 2, 2010, on the method of submitting documentation attached to the application for marketing authorization of a medicinal product
- Repeals Resulting From: Regulation of the Minister of Health of 10 February 2010 on the form of an application for a marketing authorization for a medicinal product
- Repeals Resulting From: Regulation of the Minister of Health of December 28, 2012 amending the regulation on organizational units that conduct quality testing of medicinal products and veterinary medicinal products, and the fees charged for these tests
- Repeals Resulting From: Regulation of the Minister of Health of 30 May 2003 on the organisational units that conduct qualitative tests of medicinal products and veterinary medicinal products, and the fees charged for these tests
- Repeals Resulting From: Regulation of the Minister of Health of 17 February 2003 on the monitoring of medicinal product safety