Date: 4 and 5 October 2022
Emplacement: Brussels, Belgium
Language: French/English
Qserve CRO is pleased to be attending the 4th Annual European Conference on Proactive Surveillance and Post-Market Vigilance of Medical Devices in Brussels on 4-5 October. This conference aims to provide strategies for developing robust post-market vigilance combined with a well-integrated proactive plan to improve proactive surveillance and vigilance processes. Early implementation of proactive measures will help meet regulatory requirements, gain competitive advantage and reduce the tangible costs of downstream corrective actions.
Agenda
Looking at the EU MDR and IVDR, this two-day conference will uncover some of the best strategies for streamlining complaint intake operations, detecting adverse events, handling FSCAs, managing device misuse and IFU complaints, PMCF activities, leveraging patient surveys, creating compliant PSURs, trending reports, assessing benefits and risks, creating a feedback loop for product improvement and much more.
Presentations supported by real-life case studies and practical examples will provide insight into proactive PMS and post-market vigilance strategies. This conference will allow participants to take part in highly interactive sessions supported by real-life business examples, case studies, Q&A sessions and roundtable discussions led by experienced professionals. First-hand experiences and tips will be shared to improve the end-to-end management of the proactive pharmaceutical management system and post-marketing vigilance while complying with the EU MDR and IVDR directives. Through this knowledge-sharing platform, participants will receive practical advice needed to improve their proactive PMS and vigilance systems.