Data Representative

  • Compliance with EU Data Protection Regulation
  • Representation of sponsor’s obligations

According to the General Data Protection Regulation GDPR EU 2016/679 Art. 27 all Non-EU registered companies must appoint an EU Data Representative for their clinical trial. You are required to comply with the GDPR when processing personal data of patients within the EU and when transferring personal data from the EU to a third country.

Compliance with GDPR is essential for performing clinical trials in the EU. Non-compliance leads to warnings and fines and in some countries even to criminal sanctions.

What we can do for you

  • Act as your primary contact person for the supervisory authorities and clinical trial participants, related to data protection issues

  • Oversee data processing activities and all data transfers within a clinical trial

  • Provide guidance to adhere with the requirements of the GDPR

  • Provide guidance to adhere with the requirements of the GDPR

  • Provide guidance to adhere with the requirements of the GDPR

Not sure what a specific regulation says or want to know more about the meaning behind a certain term? Visit our glossary.

Our expertise, your benefit

Lumis International has a network of data protection officers and lawyers specialised in data protection. They will apply their long-standing expertise and knowledge to help ensure that you are:

  • Compliant with EU data protection requirements
  • Represented according to GDPR article 27 
  • Fully supported in the implementation of compliance requirements

Contact our experts to find out more!

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    We look forward to being your data representative!

    Heike Schön

    Managing Director

    Phone: +49 30 235911-599

    We look forward to helping you find your best fit in outsourcing your clinical trials!