Law of March 30, 2007 amending the Law - Pharmaceutical Law and amending 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 October 28, 2002, on the liability of collective entities for offenses punishable by law.
• Amending Acts: Law of September 6, 2001, Provisions introducing the Pharmaceutical Law, the Law on Medical Devices and the Law on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products.
• Amending Acts: Law of September 6, 2001, Pharmaceutical Law.
• Amending Acts: Law of January 29, 2004, on the Veterinary Inspectorate
• Amending Acts: Law of July 27, 2001, on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products.
• Repeals Resulting From: Regulation of the Minister of Health of August 11, 2005 on the determination of groups of medicinal products and requirements for documentation of the results of research on these products
• Repeals Resulting From: Regulation of the Minister of Health of June 7, 2005 amending the regulation on the method of determining and paying fees related to the marketing authorization of medicinal products
• Repeals Resulting From: Regulation of the Minister of Agriculture and Rural Development of 6 August 2004 on the form of documentation for the retail trade of veterinary medicinal products
• Repeals Resulting From: Regulation of the Minister of Health of 4 August 2004 on the method of determining and paying fees related to the marketing authorization of a medicinal product
• Repeals Resulting From: Regulation of the Minister of Health of May 30, 2003, on the submission of documentation attached to the application for marketing authorization of a medicinal product
• Repeals Resulting From: Regulation of the Minister of Health of December 19, 2002 on requirements for the labeling of medicinal product packaging and the content of leaflets.
• Repeals Resulting From: Regulation of the Minister of Health of December 16, 2002 on the advertising of medicinal products.
• Repeals Resulting From: Regulation of the Minister of Health of 4 December 2002 on the categories of availability of medicinal products.
• Repeals Resulting From: Regulation of the Minister of Health of January 3, 2007 on the form of application for the commencement of a clinical trial of a medicinal product and for the issuance of an opinion by the bioethics committee on a clinical trial of a medicinal product
• Repeals Resulting From: Regulation of the Minister of Health of 6 July 2006 on the marketing authorization of medicinal products in non-pharmacy outlets and pharmacy points
• Repeals Resulting From: Regulation of the Minister of Health of March 3, 2006 on the amount and method of paying fees for initiating a clinical trial
• Repeals Resulting From: Regulation of the Minister of Health of June 9, 2003, on the application for marketing authorization of unprocessed pharmaceutical raw materials used for medicinal purposes, plant raw materials in comminuted form, medicinal minerals, medicinal products manufactured by industrial methods and pharmaceutical raw materials intended for the preparation of prescription and pharmacy medicines, and the list of raw materials and products
• Repeals Resulting From: Regulation of the Minister of Health of April 3, 2007 amending the regulation on the marketing authorization of medicinal products in non-pharmacy outlets and pharmacy points
• Repeals Resulting From: Regulation of the Minister of Health of March 31, 2003, on the procedure for using medicinal products in situations where there is no appropriate veterinary medicinal product authorized for marketing for a given animal species
• Repeals Resulting From: Regulation of the Minister of Health of 16 January 2003 on the forms of application for marketing authorization of a medicinal product
• Repeals Resulting From: Regulation of the Minister of Health of January 10, 2003 on the qualifications of persons dispensing medicinal products in non-pharmacy outlets, as well as the requirements that the premises and equipment of these outlets and pharmacy points should meet
• Repeals Resulting From: Regulation of the Minister of Health of 4 August 2003 on the supervision of manufacturing conditions in establishments manufacturing veterinary medicinal products
• Repeals Resulting From: Regulation of the Minister of Health of January 16, 2003 on the documentation of results of medicinal product, including veterinary medicinal product, tests and expert reports
• Repeals Resulting From: Regulation of the Minister of Health of April 30, 2004 on the detailed procedure concerning the mutual recognition procedure
• Repeals Resulting From: Regulation of the Minister of Health of June 6, 2003 on the serial pre-control of veterinary medicinal products
• Repeals Resulting From: Regulation of the Minister of Health of 10 December 2002 on determining the procedure and method of recognition by the Chief Pharmaceutical Inspector of manufacturing authorisations for medicinal products issued by an authorised body of another state.
• Repeals Resulting From: Regulation of the Minister of Health of 4 December 2002 on initial batch control.