Interactive Webcast Series Live and On-Demand
Webcode 25032518
BA/LLB, RAC, Hamish King
Cisema Ltd., Hong Kong, CHINA
CEO
Dr. Michael Gluschke
B. Braun Medical AG, Sempach, SWITZERLAND
Director Global Regulatory Affairs
Dr. Jennifer Neff
Entourage GmbH, Munich, GERMANY
Principal Consultant & Head of Medical Devices; Principal consultant with over 17 years of experience within the medical device, biotech and pharmaceutical industry. Managed international regulatgory, clinical and quality teams up to 40 direct reports. Broad experience on regulatory and clincal strategies for international product submissions. Successfull lead an IDE study for EXCOR Pediatric, the FDA PMA apprioval and the Canadian medical decice registration. Successfully lead a 505(b)(2) NDA for STERITALC based on a medical device certificate in Europe. Successfully lead several medical device registrations in Europe, US, Canada, Asia and South America. Latest projects included MDR registrations. Successfully managed MDSAP certifications as well as ISO 13485 / 21 CFR 820 QMS implementations for international product registrations. Experice in managing complex projects including effective communication with project teams and client stakeholders to meet project goals and objectives. Providing fundamental leadership skills and motivation to tram members.
05/03/-06/05/2025
05/03/-06/05/2025
Please refer to the program on our website for dates and times.
online
online
Veranstaltung - 1,290 € zzgl. MwSt.
The participation fee covers access to our Learning Space, technical support (including a pre-meeting), downloadable digital documentation, recordings of the webcast sessions and a certificate of completion.
Veranstaltung - 1,290 € zzgl. MwSt.
The participation fee covers access to our Learning Space, technical support (including a pre-meeting), downloadable digital documentation, recordings of the webcast sessions and a certificate of completion.
Verena Planitz
Conference Manager
+49 6221 500-655
v.planitz@forum-institut.de
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.
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.
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
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.
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.
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