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How to Manage Global MedTech Approval Processes from Anywhere
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Webinars are on Wednesday at 11:00 AM CET and Thursday at 11:00 AM PST

Use technology solutions to achieve and maintain market access approval for Medtech and IVD devices from anywhere.

This 45 minute webinar will cover the following:

1. What is a Global Medtech Registration Software?
2. How to keep track of product registration or approval status in each market.
3. How to get everyone to work together from home, office or the road - distributors, experts, auditors, subcontractors, authorized representative and more.
4. Real-time information, projections, and planning.
5. Cut time and eliminate redundancy - How software can help me reduce the overall time and repeated actions
6. From zero to submission file in less than 30 days - any product in any market.

Participants in the webinar will be given the opportunity to use a Global Medtech Registration system to create their product's MDR Tech File and a gap analysis.

You can choose to attend one or more of the following webinars.

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Yoav Madai (Wednesday, CEST)
Account Manager @Arazy Group Consultants
Yoav Madai is a Business Development and Account Manager at Arazy Group Consultants and has spent the last year and a half developing new territories with a focus on the Israeli medtech market. In this role, Yoav also supports East Asian companies with their journey to enter their medical and IVD devices into new markets.
Sukhi Uppal (Thursday, PST)
Account Manager @Arazy Group Consultants
Sukhi works as an Account Manager at Arazy Group assisting medical device manufacturers in North America with their goals towards global market access. He is the newest addition to our sales team and has great knowledge of the LICENSALE 2.0 system which launched last year.