Latest Updates from EMA and EC regarding Signal Detection Process Signal Detection in Pharmacovigilance is a set of activities that aim to search for and identify safety signals from a wide variety of data sources. This process wants to determine whether there are new risks associated with a particular drug, or whether risks associated with…

“When I was in my third grade of primary school, I read Madame Curie’s biography and that book really inspired me. Even though I was eight years of age, I found the scientific research very stimulating and exciting. That is what I owe my endless curiosity and passion for innovation.” says Maria Strano, Scientific Director…

In this article, we will explore the latest news about Signal Detection in Pharmacovigilance. The Signal Detection process needs to be redesigned in accordance with the integration of the EudraVigilance Data Analysis System (EVDAS). What does it mean? Let’s discover this important update together! What is Signal Detection in Pharmacovigilance? Signal Detection in Pharmacovigilance is a set…

Remote GVP Audit is a trend that is gaining traction rapidly. The COVID-19 pandemic has brought considerable changes in the management processes of several companies. This crisis has changed the way Life Sciences companies approach the GVP audits and forced them to look for new solutions that allow them to ensure business continuity and efficiently…

Dear All, As 2021 draws to a close, I would like to thank our clients, partners, and employees for working with us towards creating better lives for patients around the world. Every day, we strive to deliver a superior service to the Life Sciences community. For seQure, 2021 was a year of growth, change and transition. In June, a data-driven Contract Research Organization CROS NT, seQures sister…

Medical Device Regulation: what is it about? The EU’s Medical Device Regulation (MDR) is a hot topic in healthcare since it was officially published on 5th May 2017 and came into effect on 25 May 2017. The MDR replaces the EU Medical Device Directive (93/42/EEC) and the Directive on active implantable medical devices (90/385/EEC). Manufacturers…

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