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UK Conformity Assessed (UKCA) Marking for Medical Devices Training Course

With the June 2023 UKCA mark deadline rapidly approaching, the challenges facing Medical Device companies, Regulators and Conformity Assessment Bodies are growing. The requirements for this new UKCA mark will impact technical documentation, labelling, logistics and regulatory compliance.
The steps you need to take to prepare for the UKCA marking will depend on the current status of your business and your future market access requirements.
This seminar will provide UK and global companies practical guidance on what you need to do to continue market access or gain market access with your medical device in the UK after June 2023.

13 Jul 2022

& 3 Nov 2022 , 3 Mar 2023

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Details

Overview

With the June 2023 UKCA mark deadline rapidly approaching, the challenges facing Medical Device companies, Regulators and Conformity Assessment Bodies are growing.  The requirements for this new UKCA mark will impact technical documentation, labelling, logistics and regulatory compliance.

The steps you need to take to prepare for the UKCA marking will depend on the current status of your business and your future market access requirements.

This seminar will provide UK and global companies practical guidance on what you need to do to continue market access or gain market access with your medical device in the UK after June 2023.

Benefits in attending

  • Understand the requirements to achieve UKCA
  • Know the differences between UKCA and CE marking
  • Learn how to align your conformity assessment procedures to meet UKCA and CE marking requirements
  • Consider the requirements for the Northern Ireland market

Who should attend

Medical device professionals who wish to gain knowledge and understanding of the new UKCA requirements

Regulatory affairs managers

Medical device manufacturers

Business development managers

Programme

Welcome and introduction

UKCA Marking and your legal obligations

  • The UK Medical Device Regulations explained
  • The use of standards in the UK
  • UK guidance for medical devices

UKCA Marking explained (placement of UK CA Mark)

  • Registering as a manufacturer to sell medical devices in the UK
  • Registering medical devices in the UK
  • The role of the UK Responsible person
  • UK Conformity Assessment Bodies

Technical Files and UK Declaration of Conformity

  • UKCA Technical File Versus EU Technical documentation, differences and similaraties
  • Aligning your conformity assessment procedures

UKNI Marking and the future

  • The process in Northern Ireland
  • Proposed future changes to UK regulations

Workshop - Case Study on obtaining the UKCA Mark

Case study on obtaining the UKCA Mark

Workshop feedback

Q & A

Presenter

Janette Benaddi (More...)

Janette Benaddi is an Independent Consultant and previously the Director of Clinical & Consulting Europe for NAMSA. NAMSA is a global Medical Research Organization offering a breadth of services form preclinical to post market activities throughout the medical device product development cycle.

Janette has over 20 years’ experience of managing pre and post market clinical studies in both devices and pharmaceuticals. Janette has worked with several multinational organizations in various clinical, regulatory and marketing roles. She has extensive experience of conducting clinical studies with medical device products as well as regulatory expertise for CE marking of devices.

Janette is a registered nurse, has a BSc in Management studies, a Diploma in Company Direction, and a Diploma in Management studies, holds a teaching certificate and is a Chartered Scientist and Chartered Director. Janette sits on several committees in the device community and industry and has been an instrumental advocate of improving and advancing medical device research in the UK. Janette has published several articles relating to medical device regulation and clinical studies.

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NEW higher discounts for booking multiple places - bring your colleagues to make your training budget go further:

  • 30% off the 2nd delegate
  • 40% off the 3rd delegate
  • 50% off the 4th delegate
13 Jul 2022
Live webinar
09:30-17:00
UK (London)
13 Jul 2022
Live webinar
09:30-17:00
UK (London)
GBP 599.00
EUR 859.00
USD 970.00
+ VAT @ 20.00%
Enrol now
to attend
Live webinar
3 Nov 2022
Live webinar
09:00-17:00
UK (London)
3 Nov 2022
Live webinar
09:00-17:00
UK (London)
GBP 599 499
EUR 859 719
USD 970 814
Until 29 Sep*
Enrol now
to attend
Live webinar
3 Mar 2023
Live webinar
09:30-17:00
UK (London)
3 Mar 2023
Live webinar
09:30-17:00
UK (London)
GBP 599 499
EUR 859 719
USD 970 814
Until 27 Jan 23*
Enrol now
to attend
Live webinar

Learn more about our face-to-face and webinar training formats.

* Note the early booking discount cannot be combined with any other offers or promotional code. As such, discounts for the 2nd/3rd/4th attendees are based on the full price of the course. Please contact us for pricing if you wish to send more than 4 delegates.

Continuing professional development

This course qualifies for 6 hours for your CPD records.
More about CPD

Customised in-house training

We can customise this course to meet the requirements of your organisation and deliver it at your location and/or online.

Contact us