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October 27, 2025
On 4 September, the Court of Justice of the European Union (CJEU) delivered an important judgement in European Data Protection Board (EDPS) vs Single Resolution Board (SRB), providing fresh clarification on the status of pseudonymised data under the EU General Data Protection Regulation (GDPR).
June 9, 2025
In Part 3 of our clinical trials blog series, we explore the key GDPR considerations sponsors should address when preparing and localising Informed Consent Forms (ICFs). […]
May 12, 2025
Data Processing Agreements (DPAs) are legally required under the EU and UK General Data Protection Regulation (GDPR) whenever clinical trial sponsors use third-party vendors to process […]
April 14, 2025
In this first part of our clinical trials blog series, we explore some of the key data protection considerations that sponsors need to cover in Clinical […]
September 16, 2024
Clinical trial sponsors often face challenges when it comes to selecting the right lawful basis for clinical trial data processing. Key questions include whether the choice […]
July 24, 2023
Outlining risk reduction for CROs, sponsors & partners conducting clinical trials Clinical Trials are vital to the research and development cycle in life sciences organisations, and […]
July 19, 2023
Introduction & anonymisation techniques Effective anonymisation is an issue for many organisations, however the process remains a crucial tool in safeguarding privacy rights and ensuring […]
November 28, 2022
It is no secret that the European Union (EU) is working hard to ensure that the EU remains one of the top innovators and commercially prosperous […]
September 5, 2022
Clinical trials have been at the forefront of many peoples’ minds recently due to the COVID-19 pandemic, and the vaccination trials that were completed in record […]