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Diapharm – Regulatory Affairs, Clinical Development, Quality Management, Business Development White Papers

Diapharm – Regulatory Affairs, Clinical Development, Quality Management, Business Development

GMP services Importation into the European Union and batch release of medicinal products
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Medical device services Classification, conformity assessment, feasibility, responsibilities as manufacturer according to MDD
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Health food regulatory affairs Product claims must be scientifically proven. In particular, there are strict requirements for health claims defined in EC Regula- tion 1924/2006
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Traditional Use Registrations in Europe Traditional Herbal Medicinal Products (THMP) in accordance with Directive 2004/24/EC
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Regulatory Affairs A-consult offers world wide Drug Regulatory Affairs services.
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