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...
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.
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.
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.
Read our case study on an innovative signal detection solution implementation for a large size pharmaceutical headquartered in Italy.
In this Case Study, we analyse a recent engagement, providing GMP Audits and QP support in the EU and UK for a US biotechnology company.
Read Abiogen success story and discover how the company prepared for the upcoming obligation to monitor EudraVigilance database.
Discover how Kedrion Biopharma constituted a scalable and streamlined reporting capacity in pharmacovigilance thanks to a flexible reporting platform and a smooth implementation project.
Discover how Newcastle University moved away from paper CRFs and developed an Electronic Data Capture (EDC) and document repository system.
Read Orthofix success story to discover how the company accelerated the overall data collection and data management process with Symphony EDC.
