Webinar (in German)

UDI: Implementing global requirements
with the right strategy and software

UDI: Implementing global requirements with the right strategy and software

The Unique Device Identification (UDI) system for medical devices is already applicable in the United States and South Korea and is increasingly becoming a global challenge for medical device manufacturers with the entry into force of the European Medical Device Directive (EU MDR) in May 2021.

Many other countries, for example China, Saudi Arabia and Australia, will also introduce their own UDI regulations in the foreseeable future. Among other things, the regulatory requirements demand the transmission of UDI data to UDI databases, such as GUDID in the USA and EUDAMED in Europe. Over time, the effort required to meet the requirements of various regulatory authorities and to send product master data to UDI databases worldwide will become increasingly higher and more complex for medical device manufacturers operating in several markets. Due to the number of products, this will no longer be manageable manually.

In order to be able to handle future requirements and changes to existing regulations, efficient and above all flexible software solutions are required.

Learn in this 45-minute webinar with a live demo using the example of the UDI platform of projektraum36 how data preparation for different regulatory authorities can be efficiently implemented and thus global UDI conformity can be achieved.

DATE

Thursday, 6 May 2021, 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

Attention: Webinar will be held in German!

Our webinars are a free service for customers and interested parties of DHC.
IT service providers and consultants are excluded from participation.

The number of participants is limited. Please reserve your webinar place under:
https://register.gotowebinar.com/register/392659105049816592

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