landing page

Dear Participant,

NOVADIP would like to thank you once again for participating in the clinical trial. Participating in a clinical research is a brave and selfless decision that benefits public health and medical knowledge.

The conduct of the clinical trial implies the processing of sensitive data concerning health. To fulfill the requirements of the GDPR, additional information must be provided by NOVADIP.

NOVADIP will receive anonymized and/or pseudonymised sensitive data from the Study Doctor in the sense that the sensitive data received by NOVADIP can no longer be attributed to you.

Your data are being processed for the purpose of a Scientific Research and the processing is legally either based on your explicit consent, the execution of a contract or our legitimate interest. Only the Study Doctor can attribute the sensitive data processed during the study to you. The sensitive data we receive from the Study Doctor will be either anonymized or pseudonymised with no possibility for NOVADIP of personal identification.

NOVADIP might transfer your anonymized or pseudonymised data to companies and/or authorities outside the European Union. Appropriate safeguards will be taken and you can obtain a copy such appropriate safeguards by contacting our DPO.

Your data will be stored for all the duration of the Scientific Research including the pharmacovigilance period.

According to GDPR, you have a right to access to your data by contacting your Study Doctor. You also have the right to rectify, erase the data and restrict or object to the processing. But where personal data are processed for Scientific Research purposes, national law may provide for derogations from those rights in so far as such rights are likely to render impossible or seriously impair the achievement of the purpose and such derogations are necessary for the fulfilment of the purpose.

Your participation is voluntary and must remain free from any coercion. Even after having signed the consent prior to participate to the study, you have the right to withdraw your explicit consent at any time: the withdrawal shall not affect the lawfulness of processing based on explicit consent before the withdrawal. The provision of personal data is a necessary and contractual requirement of the clinical study. If your data are processed for a purpose other than that for which the personal data were collected, NOVADIP shall provide the Study Doctor with all the information.

The Data Protection Officer (DPO) of NOVADIP can be contacted at You also have the right to lodge a complaint before a supervisory authority. More information about the Belgian Data Protection Authority on