Farmacovigilanza: quali sono gli strumenti tecnologici innovativi a supporto della raccolta, analisi, reporting dei dati? Che cosa ci riserva il futuro?

Farmacovigilanza: quali sono gli strumenti tecnologici innovativi a supporto della raccolta, analisi, reporting dei dati? Che cosa ci riserva il futuro?
Discover the best way to adequately update the quality system for the IMPs, particularly for the aspects involving both GMP and GCP regulatory sides.
Watch this on-demand webinar and explore the key success factors and critical activities that enables setting up and maintaining an effective Pharmacovigilance system.
Watch this on demand webinar to explore what it means when regulatory authorities require a clinical trial sponsor to maintain the Trial Master File in a state of “inspection readiness”.
Watch this on demand webinar to discover the biggest challenges for pharmacovigilance in 2022 and how Gold Standard Solutions are a good match for small and medium pharma companies.
In this blog article, we are answering questions received during the Q&A session of our webinar “PSUR under the Medical Device Regulation: Practical Guide”.
Preparation of the Periodic Safety Update Report (PSUR) is one of the new requirements introduced with the Medical Device Regulation (MDR). Although it shares the name with the well-known periodic safety report for medicinal products, its format and content are...
Watch this on demand webinar to learn how to choose the right safety database in order to achieve the best results for patients and for the business.
Discover the answers to the questions asked during our webinar “Practical Advice for Your Next Remote GVP Audit”.
Watch this on demand webinar for pratical advice on planning and executing your decentralised trials and using digital measurement solutions.