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Upcoming Events Regulatory Affairs Newsletter Archive

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How to prepare for the new Post-market Surveillance Requirements in Great Britain

25 March 2025 | 09:00 and 16:00 GMT Join us for our PMS in Great Britain webinar on 25 March 2025 This insightful webinar will introduce the PMS requirements under the new regulations in Great Britain for Post-market Surveillance. Our speakers will provide an overview of the similarities and key deviations the UK PMS regulation has from EU MDR/IVDR. In addition, an update/…
Ben Kemp
February 21, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming Events Regulatory Affairs Newsletter Archive

Join the RAPS Workshop: Cybersecurity for Medical Devices 

Cybersecurity remains a top priority for medical device manufacturers   Cybersecurity Unauthorized Attend from anywhere: 25 – 26 March 2025, 9 am - 5 pm ET   This interactive virtual workshop will provide crucial insights into navigating global cybersecurity regulations and developing effective strategies to strengthen your submissions and compliance processes.   After completing this two-day workshop, you will be…
Ben Kemp
February 21, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming Events Regulatory Affairs Newsletter Archive

Explore Qserve’s Latest Training Courses & Events

Virtual Training | Person Responsible for Regulatory Compliance (PRRC) Training 📅 Date: 20 and 27 February, 2025 📍 Location: Virtual Qserve offers specialized PRRC training, aligned with MDR/IVDR requirements and MDCG 2019-07 guidance, with an option to obtain a personalized certificate demonstrating your qualification for Notified Body audits. Discover More » Live Webinar | Decoding the EU AI Act: Latest Insights and Evolving Interpretations…
Ben Kemp
February 21, 2025
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EFLM Meet the Expert – submit your case within 23 February!

6 March 2025 at h. 16.00 CET Interpretation urinalysis tests Moderator: Marielle Kaplan, Israel Learning objectives: Design the diagnostic tests for patients with suspected kidney diseases, haematuria or urinary tract infections together with the clinical units Plan verification of performance for multiple strip tests and particle analysis of urine specimens Interpret urinalysis test results against clinical background, quality of the…
Ben Kemp
February 21, 2025
Regulatory Affairs NewsletterRegulatory Affairs Newsletter ArchiveUpcoming Events Regulatory Affairs NewsletterUpcoming Events Regulatory Affairs Newsletter Archive

Webinar: Design for the Future: How to Build Sustainable Products That Support Long-Term Success

25 February - 4pm CET Do you know the carbon footprint of your product? Are you ready to provide a digital product passport to regulators? Is sustainability woven into your product design process so you can legally sell in today’s markets? It’s time to get ahead of these demands. Join us for a one-hour webinar uncovering how global regulations like…
Ben Kemp
February 21, 2025
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LIVE Webinar: Decoding the EU AI Act

Tue, Mar 4, 2025 3:00 PM - 4:00 PM GMT The EU AI Act has significant implications for medical devices and in vitro diagnostics (IVD) incorporating artificial intelligence. Join our webinar to discover the latest insights on how to integrate the requirements of the Act in an efficient manner. The webinar consists of a 45-minute presentation and a live Q&A.…
Ben Kemp
February 17, 2025
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17th International Congress in Paediatric Laboratory Medicine (ICPLM)- EuroMedLab Brussels 2025 Satellite Meeting 18th May 2005

The International Congress of Paediatric Laboratory Medicine (ICPLM) is to be held on Sunday May 18, 2025, in Brussels, as a Satellite to the main XXVI IFCC-EFLM EuroMedLab 2025. This special conference is being organized by the IFCC Committee on Emerging Technologies in Paedia­tric Laboratory Medicine (C-ETPLM) with the support of the IFCC Congresses and Conferen­ces Committee as well as…
Ben Kemp
February 7, 2025
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2025 BIVDA Regulatory Affairs Seminar agenda released

The agenda for BIVDA’s 2025 Regulatory Affairs Seminar in Birmingham on February 11 - 12 2025 has now been released. Expert figures in diagnostics regulation including David Lawson, Director of Medical Technology, Department of Health and Social Care; Robyn Meurant, Principal Consultant, ACT-IVD; and Megha Deviprasad Iyer, Director of Global Strategic Regulatory Affairs, Thermo Fisher, will lead sessions designed to…
Ben Kemp
December 9, 2024
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How do AI regulations effect medical device development?

Understand the impact of AI and emerging regulations on medical device development Thursday, December 12, 2024 | 09:00 AM (CST) - 10:00 AM (CST) Artificial intelligence (AI) is poised to transform medical engineering, but regulatory frameworks significantly impact its deployment in the healthcare industry. Join our webinar on Dec. 12, 2024, to deepen your understanding of the impact of AI…
Ben Kemp
December 4, 2024
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