2024-12-21 2024-12-21 , online online, 1,290 € plus tax Dr. Michael Gluschke https://forum-institut.com/seminar/25032518-webcast-global-medical-device-registration/referenten/25/25_03/25032518-course-global-medical-device-registration_gluschke-michael.jpg Webcast: Global Medical Device Registration

This webcast series is designed for professionals seeking to gain a clear understanding of market access for medical devices and technologies in China, Saudi Arabia, Switzerland, and the UK. The sessions are concise, focused, and include the added benefit of addressing your specific questions.

Topics
  • Comparison of country-specific regulatory requirements with those of the EU
  • Detailed overview of approval procedures and pathways
  • Insights into the challenges of market access


Who should attend
This webcast series is tailored for specialists and managers at international medical device companies who wish to enhance and update their knowledge of regulatory affairs.

It is particularly valuable for professionals working in the following departments:
  • Regulatory Affairs
  • Quality Management
  • Clinical Affairs
  • Operations Management
  • Business Development

Prerequisite: A basic understanding of medical device certification within the EU.
Aims and objectives
This webcast series comprises three live sessions focusing on the diverse regulatory requirements and approval processes for medical devices in China, Saudi Arabia, Switzerland, and the UK.

Each live webcast lasts between 1.5 and 2 hours. Join online and take advantage of the opportunity to ask questions in real time.

Presentation materials will be available for download in advance, and participants will receive a certificate of completion upon successfully passing a learning assessment.

What if you miss a live session? No problem! Recordings of all sessions will be accessible online after the live broadcast.
Your benefit

  • Gain comprehensive knowledge of specific regulatory requirements and approval processes to ensure effective and compliant product registration in international markets.
  • Understand the differences in registration procedures between the EU and other regions to optimise your global strategies.
  • Reduce compliance risks by staying informed about market access challenges and regulatory hurdles.

25032518 Course Global medical device registration

Global Medical Device Registration: China, Saudi Arabia, Switzerland and UK

Interactive Webcast Series Live and On-Demand

Benefits
  • Concise overview of international product registration
  • Short learning modules, ideal for busy workdays
  • Recordings of the live session
  • Officially certified according to ISO 9001 and ISO 21001

Webcode 25032518

Book now

JETZT Buchen

Speakers


Everything at a glance

Appointment

05/03/-06/05/2025

05/03/-06/05/2025

Period

Please refer to the program on our website for dates and times.

Please refer to the program on our website for dates and times.
Venue

online

online

Fee
Your contact

Verena Planitz
Conference Manager

+49 6221 500-655
v.planitz@forum-institut.de

Details

This webcast series is designed for professionals seeking to gain a clear understanding of market access for medical devices and technologies in China, Saudi Arabia, Switzerland, and the UK. The sessions are concise, focused, and include the added benefit of addressing your specific questions.

Topics

  • Comparison of country-specific regulatory requirements with those of the EU
  • Detailed overview of approval procedures and pathways
  • Insights into the challenges of market access


Who should attend
This webcast series is tailored for specialists and managers at international medical device companies who wish to enhance and update their knowledge of regulatory affairs.

It is particularly valuable for professionals working in the following departments:
  • Regulatory Affairs
  • Quality Management
  • Clinical Affairs
  • Operations Management
  • Business Development

Prerequisite: A basic understanding of medical device certification within the EU.

Aims and objectives

This webcast series comprises three live sessions focusing on the diverse regulatory requirements and approval processes for medical devices in China, Saudi Arabia, Switzerland, and the UK.

Each live webcast lasts between 1.5 and 2 hours. Join online and take advantage of the opportunity to ask questions in real time.

Presentation materials will be available for download in advance, and participants will receive a certificate of completion upon successfully passing a learning assessment.

What if you miss a live session? No problem! Recordings of all sessions will be accessible online after the live broadcast.

Your benefit

  • Gain comprehensive knowledge of specific regulatory requirements and approval processes to ensure effective and compliant product registration in international markets.
  • Understand the differences in registration procedures between the EU and other regions to optimise your global strategies.
  • Reduce compliance risks by staying informed about market access challenges and regulatory hurdles.

Detailed programme

Please refer to the program on our website for dates and times.

05.03.2025 09:00 - 11:00 Webcast: Global Medical Device Registration: China


03.04.2025 09:00 - 11:00 Webcast Global Medical Device Registration: Saudi Arabia


06.05.2025 09:00 - 11:00 Webcast Global Medical Device Registration: CH & UK


More informations

Free pre-meeting and technology check

You can attend one of our pre-meetings and explore our Learning Space free of charge. Registration is not required. You can find available dates for a pre-meeting in your customer portal. Click the green ‘Participate’ button in the pre-meeting in the customer portal and you will be redirected to the Learning Space.

The pre-meeting gives you the opportunity to explore our Learning Space and to familiarise yourself with the technology to start off your online training on the right foot. This is a non-binding offer for all our customers and not a prerequisite for participation. If a pre-meeting date does not suit you but you would still like a technology check, please contact us.

Access to and procedure for online events

Once you have registered for an event, we will send you the access information for your customer portal. Click here to log in to the customer portal using your email address and password. Please ensure you can access the customer portal before the day of the event.

All important or additional information and personal documents are available in your personalised customer portal. This is also where you start your online courses. If you do not have access to the customer portal yet, you can easily register here.

On the day of the event, you kick off your online training in the customer portal by clicking ‘Participate’ directly in the respective event. You will then be redirected to the Learning Space.

Learn more about our online events here.

Technical requirements

You need a reliable Internet connection to take part in our online events. To have the best possible learning experience, we recommend that you use the latest version of the Microsoft Edge or Google Chrome browsers. You will need a headset, loudspeaker or telephone to play the audio. Further information is available here. Please check beforehand that your microphone or headset and camera are working properly. Do not access our services from a VPN since there are issues with the audio over such connections.

We have integrated Zoom video conferencing software into our Learning Space for our online training courses. If you are not authorised to use Zoom, please get in touch with us so we can make alternative arrangements for you to take part in our online training.

This distinguishes our events

of 5 stars of all ratings from 2023

of 5 stars on Trustpilot = good

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We are now officially certified to ISO 9001 and ISO 21001 standard.

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