Background and Challenges The ISO IDMP (Identification of Medicinal Products) standard is an international standard established in response to the need for the unambiguous identification of medicinal products, primarily to improve information exchange and...
We are excited to announce that Arithmos will be attending the upcoming German Pharmacovigilance Day, taking place on June 6th, 2025, in Frankfurt, Germany. Organized by LS Academy, this annual event gathers Pharmacovigilance professionals, Regulatory experts, and...
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✅...
Enhance drug safety with advanced pharmacovigilance using big data, machine learning, and QSAR predictions.
Join us in Amsterdam on October 9th and 10th to connect with our Life Science experts and discuss your industry needs.
In anticipation of the new ICH GCP E6(R3) guidelines, which are due to be implemented in August / September 2024, as Arithmos we would like to discuss the evolution of clinical trial designs and proportional risks.
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.
Read this report that summarises the insights from twenty pharmaceutical industry professionals working in IT and pharmacovigilance departments
Improve efficiency, security, & data quality in clinical trials with eTMF integration. Learn how it impacts QMS & benefits of integrating with CTMS & EDC systems.
