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
23/10/2025Sponsored Webinar-Keeping submission timelines on trackFREE SPONSORED WEBINAR - For Regulatory Affairs professionals, every day matters. Missed review deadlines can mean delayed agency submissions, postponed trial starts, and lost competitive advantage. Yet many teams are still relying on SharePoint folders, email chains, and manual audit trails to manage critical submission documents. Join Ideagen to learn how companies and a leading antibody-based biotech have cut review cycles by up to 65%SPWIDEA25
28/10/2025Sponsored Webinar-Evolution of Structured Data SubmissionsFREE SPONSORED WEBINAR - The webinar covers essential terminology and concepts related to eCTD version 4.0, including key terms such as CoU (Context of Use), CoG (Context of Group), CV (Controlled Vocabulary), KW (Keywords), FWC (Forward Compatibility), and lifecycle operators, which are crucial for understanding and working with this updated electronic submission standard.SPWBEXT25
20/11/2025Sponsored Webinar-Cell & Gene Therapies-key considerationsFREE SPONSORED WEBINAR - This session will focus on the obstacles faced when navigating regulations worldwide. It aims to evaluate market dynamics and emerging trends, how regulatory authorities are providing guidance, fostering collaborations, and establishing dedicated review pathways to facilitate development, and what changes to regulations can be expected in the European Union. As a bonus, we will also take a closer look at how to realize the immense potential of gene editing within the regulatory landscape.SPWBCLAR25
25/11/2025SponsoredWebinar-Product Information prep with QRD TemplatesFREE SPONSORED WEBINAR - This webinar will explore the QRD templates and provide practical guidance on how to use them while preparing product information.   .SWBILL2025
04/12/2025Sponsored Webinar-Joint Scientific ConsultationFREE SPONSORED WEBINAR - Covering the general requirements and eligibility for Joint Scientific Consultation, which topics are covered - from a regulatory and market access perspective; how to prepare from an operational (such as briefing book) and strategic (commercial and strategic implications) perspectiveSWCLINOV25

 

Upcoming member webinars and meetings *

Start dateTitleDescription
04/11/2025Health Economics (HTA) From a Regulatory PerspectiveHealth economics and Health Technology Assessment (HTA) during the development of a new medicine are becoming increasingly important. If a medicine is to reach the patient after regulatory approval, it must undergo health economic evaluation, a basis for pricing and decisions on reimbursement. This takes place at the national level in the different EU countries. Hear from TLV and Industry about the new EU HTA Regulation (EU) 2021/2282 (HTAR) that applies from January 2025 for certain medicines, about Joint Clinical Assessment (JCA) and about HTA strategy during drug development.SWENOV25
12/11/2025Real-World Evidence in Health Technology DevelopmentTOPRA in Scotland's final meeting of 2025 to be held at the ACD Centre.  Join us, and our expert speakers, as we discuss the role of real-world (RWE) evidence in health technology development. RWE continues to gain prominence as a tool in health technology development with developers and regulators both looking to leverage the insights it can offer to support alternative pathways to market - whether it is through external control arms or post-launch evidence generation - there's a lot to be aware of.  Despite this, the regulatory considerations around RWE are often misunderstood.  Join us and our expert speakers as we look to remove some of these misunderstandings with our expert speakers.SCONOV25
13/11/2025How publishing is changing with eCTD 4.0The Regulatory Operations (RegOps) SPIN Steering Group is pleased to present “How publishing is changing with eCTD 4.0”.  This session has been designed to explore the key changes introduced by the Electronic Common Technical Document (eCTD) 4.0 and provides practical implementation examples, supported by real-world regulatory submission experience.REGOPNOV25

* Certain member webinars are open to non-members for a fee, and sometimes these webinars include two months of TOPRA Membership. 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 2019 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

Want to host a webinar? Find out more.