With the NHS requiring suppliers to ensure their labels comply with GS1 standards, this is the perfect opportunity to get ahead of the game and ensure compliance before the deadline. This one day course, designed in conjunction with Medical Device Consultancy, will outline the legal labelling requirements for any medical device being sold within the EU and US. It will explore how to design and create bar-coded labels and look at the different solutions available to companies.

You will have the opportunity to design your own label and understand the process around commercially producing this. You will also get the chance to speak with a UDI Global Lead Label producer about the challenges and difficulties linked with label creation and ensuring UDI and GS1 standards are met.

What’s in it for your business?
– Increase your company return on investment for employee training, effectively doubling your training budget
– Up-skill and gain professional recognition for your workforce
– Demonstrate excellence in skills to regulators, supply chain, customers and the public

Course content and key topics covered
– Introduction to medical device labelling requirements for EU and US standards.
– Use of symbols in labels
– Creating your own label
– UDI requirements- identification numbers, bar codes, support and resources

Who should attend
This course would be relevant for those within the following roles:
– Project leaders
– Product Managers
– Quality Assurance
– Technical/Artwork/Manufacturing roles
– Regulatory Personnel

By attending this course you will
– Gain an understanding of the regulatory requirements and how they impact you
– Understand the bar code symbols you should use and how to ensure barcodes are at the required standard

Delegate fee
Member fee: £280.00
Non-member fee: £380.00 *Eligible SMEs will receive a 50% discount on the listed delegate fee.

To register or for more information please contact Sarah Wootton – 0121 452 5630