Please complete and submit the form below to provide your initial information as enquiry to QMD Services. Please note, only fully completed forms can be processed.
We gladly accept submissions of technical documentation for conformity assessment activities acc. to Regulation (EU) 2017/746 on in vitro diagnostic medical devices and Regulation (EU) 2017/745 on medical devices in English and German.
For German submissions, acceptance is subject to the availability of reviewers with the appropriate language skills.
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To provide the best experiences, we use technologies like cookies to store and/or access device information. Consenting to these technologies will allow us to process data such as browsing behaviour or unique IDs on this site. Not consenting or withdrawing consent, may adversely affect certain features and functions.
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The technical storage or access is required to create user profiles to send advertising, or to track the user on a website or across several websites for similar marketing purposes.
