Recorded: 2 December 2021 (14:00 - 15:30 UK time)
What’s this webinar about?
Via an expert panel discussion and a Q&A, this webinar explores the role standards play in tackling NHS-wide patient safety concerns and how standards can benefit safe NHS procurement going forward.
The discussion focuses on the supply chain and the regulatory and systematic aspects of ensuring the safety of medical technologies in the healthcare system. We look at examples from national patient safety investigations, essential specifications for clinical and product assurance, and human factor engineering best practices.
Who is this webinar for?
- Medical device and health technology designers and manufacturers
- NHS procurement leads
- NHS patient safety leads
What will participants gain?
- A stronger understanding of how standards can increase patient safety
- Information on how standards can help manufacturers access the NHS supply chain and procurement professionals specify safer devices and technologies
- Highlight opportunities for new standards to address patient safety challenges
Agenda
14:00 - 14:10 Welcome and introduction - Rob Turpin, Head of Sector for Healthcare, British Standards Institution (BSI)
14:10 - 14:40 Perspectives from the panellists on the topic - Tracey Cammish, Clinical Intelligence and Safety Lead, NHS Supply Chain, Janine Jolly, Group Manager - Devices Safety and Surveillance, Medicines and Healthcare products Regulatory Agency (MHRA), Sarah Jennings, National Patient Safety Clinical Lead for Medical Devices, NHS England, Nichola Crust, National Investigator, Healthcare Safety Investigation Branch (HSIB), Chris Frerk, Consultant Anaesthetist, Northampton General Hospital and Clinical Human Factors Group (CHFG) Trustee
14:40 - 15:30 Live Q&A session
15:30 Closing remarks
To learn more about how standards can help tackle patient safety concerns, please watch the webinar recording now.