Webinars

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TOPRA hosts a wide range of webinars over the course of the year that are led by experts.

You can take part in our webinars live, with the opportunity to ask your own questions and participate in discussion, or you can choose to view one of our archived webinars in your own time.

About access to TOPRA webinars

TOPRA members have access to all live webinars, with member webinars typically free to view and sign-up for paid webinars available at a special member rate. Non-members are not eligible to register for member webinars except in rare instances where indicated.

Discounted Places

A limited number of discounted webinar places are available for those:

See our individual webinar registration pages for more information about discounted pricing.

Upcoming webinars open to all

Begin DateTitleDescription
08/09/2026MDR: Biocompatibility, Clinical Evaluation & Risk AssessmentJoin Billev Pharma East for a free webinar on bringing biocompatibility, clinical evaluation and risk management together into one coherent, audit-ready MDR technical file. Drawing on regulatory and clinical experience, we'll cover current expectations under ISO 10993-1, MEDDEV/MDCG guidance and ISO 14971 and practical strategies for making your evidence package hold up under scrutiny. For regulatory affairs, quality and clinical professionals working on MDR technical files.BILLSEPT26
06/10/2026Structure Content, Managed Data and AIStatic, document-based systems often limit the flow of regulatory information, slowing down processes and increasing compliance risk. The joint vision of cormeo and its brands EXTEDO, Docuvera, Rote Liste, and medicines.ie is to move beyond disconnected files and manual processes - imagine structured components, master data, and submissions flow through streamlined workflows until successful approval by the health agency.CORM092026
28/10/2026European MedTech Market: One Approval Isn’t EnoughDA approval often creates a false sense of readiness for MedTech companies entering Europe, where underestimating regulatory and clinical differences leads to Notified Body delays, evidence gaps, and unpredictable timelines under MDR and IVDR. Building on QbD Group's Landing in Europe whitepaper, this webinar explains why EU entry demands a different approach, covering clinical evidence expectations, Notified Body interactions, and the full lifecycle from gap assessment to CE marking and post-market compliance. Register to assess your true EU readiness, avoid costly delays, and learn what it really takes to succeed in Europe.QBDOCT26

 

Upcoming SPIN and IN webinars*

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* Certain member webinars are open to non-members for a fee. Please see the individual member webinar event page to find if it is available for non-member registration.

Archived members-only webinars

Most members-only webinars going back to the start of 2024 are available on demand to members.

Visit the members-only webinars archive to view them. (Member log-in required) 


On-demand webinars

Visit our On-demand Learning section for a complete list of pre-recorded webinars available for purchase.

Sponsored Webinars

Reach the regulatory professionals who matter most to your business.


TOPRA's sponsored webinars place your expertise directly in front of a highly engaged audience of regulatory affairs professionals across Europe and beyond. Share your insights, build credibility, and get your brand in front of the decision-makers who count.

Ready to get started? Contact us to find out more