{"id":2115,"date":"2024-11-22T11:02:38","date_gmt":"2024-11-22T10:02:38","guid":{"rendered":"https:\/\/www.pharmanager-development.com\/?post_type=sector&p=2115"},"modified":"2025-02-03T12:09:01","modified_gmt":"2025-02-03T11:09:01","slug":"herbal-medicines","status":"publish","type":"sector","link":"https:\/\/www.pharmanager-development.com\/en\/secteur\/herbal-medicines\/","title":{"rendered":"Herbal Medicines"},"content":{"rendered":"\n
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Accueil<\/a><\/span><\/span><\/div> <\/div>\n
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Herbal Medicines<\/span><\/h1>\n

Herbal medicines are a natural and scientifically recognized alternative in the field of healthcare. At Pharmanager Development, we support you through every step necessary to ensure market authorization (MA) for your products, in compliance with Directive 2001\/83\/EC and Directive 2004\/24\/EC.<\/span><\/p>\n

Our expertise helps you navigate regulatory and strategic challenges, ensuring that your products meet safety, quality, and efficacy requirements. Whether your goal is to enter the European market or international markets, we are here to ensure the success of your projects.<\/span><\/p>\n

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What regulations apply to herbal medicines?<\/h2>\n

By adhering to these regulations, your products can benefit from a solid legal framework for marketing within Europe.<\/p>\n <\/div>\n <\/div>\n

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Directive 2001\/83\/EC<\/strong><\/h3>\n <\/div>\n
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This Community code sets the rules for human medicines, including those containing medicinal plants. It defines the requirements for market authorization, ensuring their safety and efficacy.<\/p>\n <\/div>\n <\/div>\n

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Directive 2004\/24\/EC<\/strong><\/h3>\n <\/div>\n
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It specifies the conditions for traditional herbal medicines, simplifying their registration while maintaining strict quality and traceability standards.<\/p>\n <\/div>\n <\/div>\n <\/div>\n <\/section>\n\n\n

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Preparation of MA Dossier Modules
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Preparation of MA Dossier Modules
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Enregistrement des dossiers\u00a0<\/span><\/h3>\n \n <\/span>\n <\/span>\n <\/span>\n
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Gestion de toutes les d\u00e9marches administratives et r\u00e9glementaires.<\/p>\n <\/div>\n <\/div>\n

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Interface with Competent Authorities\u00a0<\/span><\/h3>\n \n <\/span>\n <\/span>\n <\/span>\n
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We manage communications with the ANSM, EMA, or other international organizations.<\/span><\/p>\n <\/div>\n <\/div>\n

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Response to Instruction Measures\u00a0<\/span><\/h3>\n \n <\/span>\n <\/span>\n <\/span>\n
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We analyze and address the questions raised by the authorities.<\/p>\n <\/div>\n <\/div>\n

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Development of New Products<\/span><\/h3>\n \n <\/span>\n <\/span>\n <\/span>\n
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