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    Handling and brokering of medicinal products

    28.04.2017
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    Handling and brokering of medicinal products are regulated by the following general laws and regulations (legislation available in English):

    Handling of medicinal products in pharmacies is additionally regulated by the following regulations (legislation available in English):

    Handling of medicinal products by wholesalers and manufacturers is additionally regulated by the following regulations (legislation available in English):

    The national Parliamentary law Medicinal Products Act stipulates (legislation available in English):

    • The wholesale distribution of medicinal products and active ingredients for human use and the brokering of medicinal products for human use must comply with the good distribution practices established on the basis of Article 47(4) and Article 84 of Directive 2001/83/EC of the European Parliament and of the Council
    • The manufacturing of medicinal products and active substances must comply with the good manufacturing practice of the European Economic Area drawn up on the basis of Article 47 of Directive 2001/83/EC of the European Parliament and of the Council and Article 51 of Directive 2001/82/EC of the European Parliament and of the Council on the Community Code relating to veterinary medicinal products (OJ L 311, 28.11.2001, pp. 3–67)


    The translations of legislation published on our web site may not reflect the latest versions in force and may include provisions which have been amended or declared invalid. Not all regulations related to handling of medicinal products are available in English. Please send your request for information to info@ravimiamet.ee