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23 September 15:00 - 16:30

 

Welcome to a complimentary webinar that aims to inspire Sweden-based, small & medium sized companies (SMEs) how to navigate the transition towards alignment with the new EU Medical Device Regulation (MDR).

Rather than being a formal MDR training session, the webinar - hosted by AstraZeneca’s BioVentureHub – will provide you with insights, examples and experiences on how big pharma, global medtech and SMEs are planning and navigating their MDR journeys depending on product profiles and market strategies. 

Webinar overview
• AstraZeneca –AstraZeneca's response to the MDR impact on Drug-Device Combination products
• Mölnlycke – global medtech way of working
• Devicia - SME's perspective 
• Q&A

You are more than welcome to send us questions or specific topics/issues that you’d like us to bring up during our webinar. You will receive a webinar link by email before the webinar. 

We hope you will be able to join us!
AstraZeneca BioVentureHub

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Everything you need to know

When: 23 September, 3:00-4:30 AM (Stockholm time, CET +1)

Where: Online webinar

How: The webinar is free of charge and will be held in English

Speakers: Johanna Lindström (Mölnlycke), Christina Lewing (Mölnlycke), Jenny Fäldt (Mölnlycke), Tim Chesworth (Astra Zeneca), Elisabeth Liljensten (Devicia AB) och Sofia Nordgren (Devicia AB)

Who should attend: Swedish-based, small & medium sized companies with interest in the new EU Medical Device Regulation

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Organized by AstraZeneca BioVentureHub in collaboration with