Category: Laws / Regulations of Germany

Medicinal Products Act (Laws / Regulations of Germany) Section 12 Empowerment in respect of labelling, package leaflet and package sizes (1) The Federal Ministry is hereby empowered,

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Medicinal Products Act (Laws / Regulations of Germany) Section 11a Expert information (1) The pharmaceutical entrepreneur shall be obliged to make available upon request to physicians,

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Medicinal Products Act (Laws / Regulations of Germany) Section 11 Package leaflet (1) Finished medicinal products that are medicinal products within the meaning of Section 2

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Medicinal Products Act (Laws / Regulations of Germany) Section 10 Labelling (1) Finished medicinal products that are medicinal products within the meaning of Section 2 sub-section 1 or sub-section 2 number 1,

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Medicinal Products Act (Laws / Regulations of Germany) CHAPTER TWO Requirements on medicinal products Section 5 Prohibition of unsafe medicinal products

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Medicinal Products Act (Laws / Regulations of Germany) CHAPTER ONE Purpose of the Act, definition of terms, scope Section 1 Purpose of the Act

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Full citation: Medicinal Products Act in the version published on 12 December 2005 (Federal Law Gazette [BGBl.]) Part I p. 3394, last amended by Article 11 of the Act of 6 May 2019 (Federal Law Gazette I p. 646)

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Stock Corporation Act (Laws / Regulations of Germany) Part 6 Group accounting Sections 329 to 336 (repealed) Section 337 (repealed) Section 338 (repealed) Book 4 Specific provisions, penal provisions, and final provisions Part 1

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Stock Corporation Act (Laws / Regulations of Germany) Part 4 Expulsion of minority stockholders Section 327a Transfer of shares of stock in return for cash settlement

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Stock Corporation Act (Laws / Regulations of Germany) Part 3 Integrated companies Section 319 Integration (1) The general meeting of a stock corporation may resolve to integrate

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