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It all started with the story of Marie Curie that I read when I was 8 | Interview with Maria Strano
“When I was in my third grade of primary school, I read Madame Curie’s biography and that book really inspired me....
EudraVigilance and Signal Detection in Pharmacovigilance: What’s new?
The Signal Detection process needs to be redesigned in accordance with the integration of the EudraVigilance Data Analysis System (EVDAS).
Discover the latest news about Signal Detection in Pharmacovigilance.
Industry Report | Pharmacovigilance and Technologies: an Insider Look at State of the Art, Challenges and Future
Download our Industry Report and discover a new perspective to interpret the expected impact of emerging technologies on the future of pharmacovigilance.
Why choose Remote GVP Audit?
Remote GVP Audit is a trend that is gaining traction rapidly. The COVID-19 pandemic has brought considerable changes...
A Letter from Our CEO
Our CEO Paolo Morelli would like to thank our clients, partners, and employees for working together in 2021 towards creating better lives for patients around the world.
Read some thoughts on the year and Arithmos plans for 2022.
How Can Decentralised Trials Foster Patient-centricity: An Insider Look
Read this interview to discover how Life Sciences companies can embrace patient-centricity in R&D in a way that benefits patients the most.
Risk Management Requirements for Post-Market Surveillance for Medical Devices
Medical Device Regulation: what is it about? The EU’s Medical Device Regulation (MDR) is a hot topic in healthcare...
Webinar Q&A | PSUR under the Medical Device Regulation: Practical Guide
In this blog article, we are answering questions received during the Q&A session of our webinar “PSUR under the Medical Device Regulation: Practical Guide”.
How to Embrace Digital Transformation in Life Sciences
Read this interview to discover how Life Sciences businesses can embrace Digital Transformation effectively and harness its power.
The MDR: Medical Device PSUR as per Regulation (EU) 2017/745
Regulation (EU) 2017/745 also known as the MDR, applicable since May 26th 2021, introduced a new obligation for the...
Transforming Your Pharmacovigilance
Learn how to choose the safety database that will transform your pharmacovigilance department.
eTMF – Your Key to Inspection Readiness
Discover how evolving beyond paper-based processes and adopting an eTMF help ensure inspection readiness.