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.
Webinars
Webinar (Italian language) | Aspetti bibliografici e bibliometrici nel Life Science: dalla carta all’intelligenza artificiale
Webinar | Aspetti bibliografici e bibliometrici nel Life Science: dalla carta all’intelligenza artificiale. Potenziali implicazioni per i ricercatori e gli operatori del settore.
Webinar (Italian language) | Linea guida EMA sui sistemi computerizzati e i dati negli studi clinici: riflessioni operative
Webinar | Linea guida EMA sui sistemi computerizzati e i dati negli studi clinici: riflessioni operative
On Demand Webinar (Italian language) | La Farmacovigilanza tra presente e futuro
Farmacovigilanza: quali sono gli strumenti tecnologici innovativi a supporto della raccolta, analisi, reporting dei dati? Che cosa ci riserva il futuro?
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.
On Demand Webinar | Key Success Factors for Setting Up an Effective Pharmacovigilance System
Watch this on-demand webinar and explore the key success factors and critical activities that enables setting up and maintaining an effective Pharmacovigilance system.
On Demand Webinar | Inspection Readiness: is your company ready?
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”.
On Demand Webinar: How Small to Medium Pharma can address the increasing Challenges in Safety Case Management
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.
Webinar Q&A | PSUR under the Medical Device Regulation: Practical Guide
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”.
On Demand 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...
