Member price: Free
Non-Member price: Free
Overview
Unique Device Identification (UDI) forms the foundations of many global healthcare regulations. As a supplier, it is important to know exactly what you need to do to comply and understand what doing so means in clinical settings, beyond the realms of the healthcare supply chain.
To ensure you are up to speed on how to use and implement GS1 standards to meet UDI requirements, we have developed a short half day programme that will provide you with an in-depth understanding of what you need to do.
Join us to discover how the seemingly small act of uniquely identifying your products has a huge impact on transforming patient care.
To find out more about the session and speakers, visit our web page to view the agenda.
Who should attend from manufacturer and supplier organisations?
- Finance professionals (including: chief financial officer, financial and credit controllers, and finance managers)
- Business development professionals (including: business development manager, account managers, director of and head of sales, commercial managers)
- IT, data and systems leads (including: IT directors and managers, finance systems managers, technical directors and EDI coordinator)
- Managing directors and operational leads
- Quality and regulatory compliance leads
- Supply chain professionals
- Medical professionals
Who should attend from trusts and NHS arm's length bodies?
- Finance professionals (including: directors of finance and finance managers)
- Procurement professionals (including: directors and assistant directors of procurement, heads of procurement, procurement and e-procurement managers, and operations procurement leads)
- Systems management leads (including: financial systems support professionals, procurement systems managers, and systems project accountants)
- Digital programme managers
- Scan4Safety leads and programme managers
- E-commerce managers
- Healthcare regulators
Learning outcomes
- Discover the importance of accurate product identification using GS1 standards
- Explore the impact of UDI beyond the supply chain
- Why this is vital for product recalls and patient safety
- How UDI underpins efficiencies within the purchase to pay process
- What this means for hospitals system interoperability
- How UDI enables full product traceability and where this fits into healthcare’s national integration strategy
- Understand how to use GS1 standards to meet regulatory requirements for EU Medical Device Regulations (EU MDR) and prepare for forthcoming UK UDI legislation (e.g. the Medicines and Medical Devices Act)
- Find out how to get started on how to adopt and implement GS1 standards for UDI