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.
Arithmos
On Demand Webinar | Clinical Data and Study Documents: operational aspects to support Inspection Readiness
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.
Arithmos attends the World Drug Safety Congress Europe 2024
Join us in Amsterdam on October 9th and 10th to connect with our Life Science experts and discuss your industry needs.
Press Release | New Arithmos Office in Boston, Massachusetts
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.
The New ICH E6 (R3) Guidelines: Impact on Clinical Trials
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.
Case Study | Arithmos Transforms Medical Device Company’s Data Landscape with a Data Warehouse Implementation
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.
Corso Pratico di Alta Formazione in “Laboratori di GxP (Good for Practice) – Requisiti per svolgere la funzione di QA e GCP Auditor”
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.
Report | Pharmacovigilance 2.0: Leveraging Analytics and Automation
Read this report that summarises the insights from twenty pharmaceutical industry professionals working in IT and pharmacovigilance departments
eTMF Integration: Benefits and Impact on QMS
Improve efficiency, security, & data quality in clinical trials with eTMF integration. Learn how it impacts QMS & benefits of integrating with CTMS & EDC systems.
Case Study | Ensuring GLP Compliance Through Third-Party Vendor Audits
Worried your GLP compliance is impacted by a vendor’s restructuring process? Learn how we manage third party vendor audits to ensure process and data integrity.
