2022

Privacy compliance and clinical trials

by cyb2025

SOPHIE BERNARD
PRINEOS srl, Milano, Italy

INTRODUCTION
Clinical trials are challenging by definition. Even though any clinical research entails a certain degree of uncertainty regarding its potential success, several clinical trials challenges come with opportunities for improvement and are major drivers of innovation.

 

PRINEOS srl proposes this column with the aim of spreading greater awareness about challenges and opportunities for improvement in clinical trials, addressing several crucial topics in this context.
Our journey starts with the topic “Privacy Compliance and Clinical trials” as privacy compliance has been (and may still be) quite challenging for all stakeholders involved in clinical research, considering also the lack of a general legal framework on this subject.

 

ABOUT THE AUTHOR

Sophie Bernard (Privacy & Data Protection Manager, PRINEOS srl) has grown a solid experience in the field of data protection in healthcare and contract research industries and defends that understanding the rules applicable to clinical research is essential to find the right balance between scientific progress and protection of patients’ rights and freedoms.
PRINEOS srl is a new strategic consulting company born and raised by passion, leveraging on a team with more than 25 years of expertise in the Life Sciences.
Our goal is to improve and innovate Clinical Research in Healthcare providing services on: Biostatistics, Medical Affairs, Regulatory and Legal Affairs.

Login