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Annex II and III of Regulation (EU) 2017/745 define in general which technical documentation must be prepared in a scientific, objective and clear way. Cebis has a long experience in the field on how documentation must be prepared and, thanks to the team specialized in the technical documentation of medical devices, can support companies in the rapid and effective compilation of the necessary technical documentation.
Even if you are still in the planning stages of your project, you are more than welcome to submit a request to us. We can assist you with a quotation or create a proposal for you based on the minimum information you can provide.
