There are many different languages in Europe, and certain elements on the label have to be translated into the local language(s) of the country(ies) you want to sell your product in. We cooperate with translation companies that can translate these elements for you! We can also help you if you would like to translate any other documents.
Contact us to find out more about the Translation service and to receive a quote.
lunes, 10 de noviembre de 2014
miércoles, 5 de noviembre de 2014
Guidance on labelling requirements
Labelling is one of the most important components of the product both in terms of sales, and in terms of compliance with the EU Medical Devices Directive 93/42/EEC (MDD), Active Implantable Medical Device Directive 90/385/EEC (AIMDD) or In Vitro Diagnostic Medical Device Directive 98/79/EC (IVDD). Many companies are having problems determining the labelling requirements; which information has to appear on the product labeling, what is required, what isn’t, and what is prohibited.
Revipharm can provide guidance on the labeling requirements and review your labels to ensure their compliance with the applicable legislation.
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