Stay ahead of inspections with Arithmos QA Consultancy. The Challenge: The pharmaceutical and life sciences industry is experiencing an uptake in FDA activities across the EU, driven by developments like the Mutual Recognition Agreement (MRA) between the FDA and EU...
Explore, in this case study, how Arithmos helped a medical device company overcome data silos and fragmented data to achieve a single source of truth for informed decision-making.
Improve efficiency, security, & data quality in clinical trials with eTMF integration. Learn how it impacts QMS & benefits of integrating with CTMS & EDC systems.
This webinar delves into challenges, with insights into how technology-enhanced solutions can revolutionise signal detection practices.
Join us in Madrid from the 4th – 5th of June to connect with our Life Science professionals and discuss your industry needs.
Arithmos welcomes Massimo Raineri to the team. Find out more about Arithmos’ new Senior Consultant, Clinical Business Partner.
Discover, in our on-demand webinar, useful information to better manage IDMP-related activity to comply with regulatory requirements.
In this Whitepaper, we analyse the current and future changes in the pharmacovigilance field, and how technology plays a critical role.
A look at RWD and RWE, describing differences and their significant support to medicines evaluation and regulatory decision-making in Life Science.
