Together with our GLP Auditor Michelle Anderson, we delve into the significance of test item characterisation in GLP.
Arithmos expands its UK presence with new office in Pickmere, Knutsford to accommodate its business growth.
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.
We are pleased to announce that this year our Quality Assurance business unit, The CQA Company, will be exhibiting at the RQA's 2023 International QA Conference. Join us 1st-3rd November in Belfast and meet our QA Manager, Ceri Thornley, and Head of Marketing and...
On Demand Webinar (Italian language) | I sistemi integrati per la gestione delle attività nel mondo dell’industria biomedicale: il caso VEEVA
Quali sono i benefici dei sistemi integrati, cloud based, per il mondo Life Sciences? Scopri, in questo webinar, le esperienze dirette di alcune importanti realtà farmaceutiche.
Investing in a regulatory mock inspection demonstrates a serious commitment to patient safety, data integrity, and regulatory compliance.
On Demand Webinar | Investigational Medicinal Products in the new era of Clinical Trial Regulation 536/14: How to manage them?
Discover the best way to adequately update the quality system for the IMPs, particularly for the aspects involving both GMP and GCP regulatory sides.
We analysed remote GVP audits during the pandemic and what industry leaders are saying about its future potential in a post-pandemic world.
Remote GVP Audit is a trend that is gaining traction rapidly. The COVID-19 pandemic has brought considerable changes in the management processes of several companies. This crisis has changed the way Life Sciences companies approach the GVP audits and forced them to...
From on-site audits to remote audits The global spread of COVID-19 amongst other challenges has resulted in travel and work restrictions. This crisis has changed the way Life Sciences companies approach the GxP audits and forced them to look for new solutions that...