We are pleased to announce that Arithmos will be attending the 64° AFI Symposium in 2025. Join us in Rimini, Italy from the 11th-13th June at Stand 87 to discuss advancements in pharmaceutical sciences, digital transformation, and innovative therapeutic approaches....
For the third consecutive year in a row, we are very proud to be Veeva Services Partner for the Development Cloud. We are thrilled to share our newest approved Services Alliance Partner Certifications: ✅ Business Process/Strategy✅ Implementation Support✅ Post...
Save the Date: May 28-30, 2025 Arithmos is excited to announce our participation in the 32nd GIQAR Congress, taking place at the TH Lazise - Hotel Parchi del Garda. This prestigious event will bring together industry leaders and experts to discuss the latest...
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...
Over the past six years, the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) has been working on reinventing the E6 Good Clinical Practice (GCP) guideline that was first introduced in 1996 and revised in 2016....
Our client, a specialist company based in the US working to develop treatments within a specific therapeutic area, requested a service provider qualification audit of a contract research organisation (CRO) which they were using to support the delivery of two active clinical trials.
Join us in Brighton on the 6th-8th of November to connect with our experts and discuss your Quality Assurance needs.
New Webinar: get useful insight into how QA is important for data and documents that drive a decision to approval, commercialisation, and prescription of medications.
Italian Language | In collaborazione con il progetto DARE della Fondazione DARE, il corso si configura come un
primo step di formazione teorica per il raggiungimento della qualifica prevista dalla Normativa vigente
per Auditors GCP.
Improve efficiency, security, & data quality in clinical trials with eTMF integration. Learn how it impacts QMS & benefits of integrating with CTMS & EDC systems.
