GDPR Recital 161 Consent for participation in scientific research clinical trials
For the purpose of consenting to the participation in scientific research activities in clinical trials, the relevant provisions of Regulation (EU) No 536/2014 of the European Parliament and of the Council (1) should apply.
Guidelines 9/2020 on relevant and reasoned objection under Regulation 2016/679 Paragraph 3.2.3 Risks to free flow of personal data within the Union 44. Where the objection will refer to this particular risk, the CSA will need to clarify why it …
Guidelines 9/2020 on relevant and reasoned objection under Regulation 2016/679 Paragraph 3.2.2 Risks to fundamental rights and freedoms of data subjects 39. The issue at stake concerns the impact the draft decision as a whole would have on the data …
Guidelines 9/2020 on relevant and reasoned objection under Regulation 2016/679 Paragraph 3.2.1 Meaning of “significance of the risks” 35. It is important to bear in mind that the goal of the work carried out by SAs is that of protecting …