DHC & LSA Websession (in German)

UDI: Implementing global requirements
with the right strategy and software

UDI: Implementing global requirements with the right strategy and software

As a member of the Life Sciences Alliance, we are organising this web session together with p36.

The Uniform Device Identification (UDI) system for medical devices is already applicable in the United States, South Korea as well as China and is increasingly becoming a global challenge for medical device manufacturers due to the EU MDR / IVDR, among others.
Many other countries, for example Saudi Arabia and Australia, will also introduce their own UDI regulations in the foreseeable future. Among other things, the regulatory requirements include the submission of UDI data to UDI databases, for example GUDID in the USA and EUDAMED in Europe. Over time, the effort to meet the requirements of different regulatory authorities and to be able to send product master data to UDI databases worldwide will become increasingly higher and more complex for medical device manufacturers who are active in several markets. Due to the number of products, this will no longer be manually manageable.
In order to be able to handle future requirements and changes to existing regulations, efficient and above all flexible software solutions are required.
Learn how data preparation for various regulatory authorities can be efficiently implemented and thus global UDI compliance can be achieved with the help of a live demo using the UDI Platform from our partner company p36 as an example.

DATE

Friday, 4 February 2022, 10:00 – 10:45 a.m.
No time on this date? Then simply register anyway and secure your access data for the free podcast! You will then automatically receive these shortly after the webinar.

TARGET GROUP OF THE WEBINAR

This webinar is aimed at specialists and managers from the medical technology sector who are concerned with the optimisation of processes in the registration – especially due to increasing requirements such as UDI

CONTENT OF THE WEBINAR

  • Overview of global UDI requirements
  • Strategic considerations and system requirements for a global UDI setup
  • System demo: Data preparation and transmission to various regulatory authorities using the UDI platform as an example

YOUR BENEFIT

  • Over 20 years of experience in the implementation of SAP in the pharmaceutical and medical technology industry
  • You will get an understanding of the future-oriented implementation possibilities of UDI based on the SAP Cloud Platform with the UDI platform of projektraum36
  • Interactive exchange with our experienced consultant and other webinar participants

TECHNICAL REQUIREMENTS

The webinars are online seminars. All you need to participate is a PC with an Internet connection and loudspeakers. Alternatively, the sound transmission can also be made by telephone, while you can follow the image presentation via your browser. The webinars are interactive, i.e. you can ask questions at any time.

PARTICIPATION AND REGISTRATION

The websession will be held in German. If you only speak English, please contact us via email for a personal online appointment (consulting@dhc-gmbh.com). We are looking forward to meeting you!

This webinar is a free service for customers and prospects of DHC and the Life Sciences Alliance.
IT service providers and consultants are excluded from participation.
The number of participants is limited. Please use the following link to register for our websession:
https://attendee.gotowebinar.com/register/1540265577196683534

After registering, you will receive a confirmation email with all the information you need to participate in our web session.

SAP and other SAP products and services mentioned in the text as well as the respective logos are trademarks or registered trademarks of SAP SE in Germany and other countries worldwide.

 

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