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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 […]