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). […]
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 […]
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 […]
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 […]
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 […]
Introduction & anonymisation techniques Effective anonymisation is an issue for many organisations, however the process remains a crucial tool in safeguarding privacy rights and ensuring […]
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 […]