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....
We are pleased to announce that this year Arithmos will be attending DIA Europe, a global association that mobilises life science professionals from across all areas of expertise. 📅 Save the Date: 18th - 20th March 2025 📍 Location: Basel, Switzerland 📌...
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.
Enhance drug safety with advanced pharmacovigilance using big data, machine learning, and QSAR predictions.
Join us in Brighton on the 6th-8th of November to connect with our experts and discuss your Quality Assurance needs.
Watch our on-demand webinar and learn more details about the Italian Ministerial Decree 20/11/2021 on the transfer of data of independent clinical research.
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.
Join us in Amsterdam on October 9th and 10th to connect with our Life Science experts and discuss your industry needs.
Arithmos is thrilled to unveil our latest milestone: the inauguration of a new office in the vibrant city of Boston, Massachusetts which is home to so many of our Biotech and Pharmaceutical clients.
