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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.

Note: TOPRA members have access to all live webinars; non-members are not eligible to register for members-only webinars.

Upcoming webinars open to all

Begin DateTitleDescription
15/09/2020Regulatory Environment in Russia and the EAEUGet an overview on the regulatory framework for medicines and processes in Russia and the Eurasian Economic Union (EAEU)!WEBGDRU
14/10/2020Genesis of Medical Device Regulatory IntelligenceThis webinar is designed to support those new to the Regulatory Intelligence concept in the medical device sector and to provide a foundational plan to anyone looking to take their first steps in assuming primary responsibility for regulatory intelligence in their organisation.WEBRIMD
15/10/2020Medical Device Regulatory Intelligence for Decision MakersRegulations for a pharmaceutical or medical device product not only differ across the globe but are constantly evolving too. Proactively acting in a very challenging regulatory scenario is crucial for medical device and in vitro diagnostic companies and decisions need to be supported by accurate and timely information. Join our webinar to understand why regulatory intelligence matters for global regulatory activities and how it can impact business decisions!WEBMDRIA


Members-only webinars

Start dateTitleDescription
15/07/2020CMC SPIN Webinar: CMC Filings in JapanTOPRA's CMC SPIN is pleased to invite members to a webinar on CMC filings in Japan. This TOPRA webinar will be an overview of the regulatory process for filing clinical and registration submissions for small molecules, and will include a comparison of the process in Japan to other regions and the challenges encountered.CMC22JUN20
17/07/2020Reg Ops SPIN Webinar: The EAEU ContextThe TOPRA Regulatory Operations SPIN are pleased to announce our next webinar, in which we will have the pleasure of hosting Karl-Heinz Loebel (Director, Principal Consultant at PharmaLex) as he delivers insight into the EAEU procedure.EAEUJUL20


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

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Webinar: ATMPs, Human Tissues and the MDRThis webinar will give you sufficient understanding to classify new products and technologies containing human tissues or cells and to understand the impact of such products in a portfolio.ATMP2019
Webinar: EMA Article 58 Pathway for Global Health MedicinesThis webinar discussion given by Dr Agnes Saint-Raymond, Head of International Affairs Division, Head of Portfolio Board, European Medicines Agency gives a comprehensive overview of the added value and opportunities offered by EU-Medicines4All/Article 58 right through the medicine development lifecycle.WEBARTC58
Webinar: Quality/CMC Considerations for ATMPsThis webinar will provide an overview of the quality/CMC considerations with respect to clinical trial applications and marketing applications for advanced therapy medicinal products (gene and cell therapy products). This will include an outline of the current guidance for these product types for the EU and the USA and specific challenges for cell-based therapies, gene therapies and combined ATMPs.WEBATMPCMC
Unannounced Audits - A Practical Guide for ManufacturersAre you ready for an unannounced audit by your Notified Body? This webinar can help managers and staff to be prepared.WEBAUDIT
Webinar: The Regulation of Biotechnology ProductsThis webinar will provide an introduction to biotechnology products for regulatory affairs professionals.WEBBIOIC2
Webinar: Updates on China Regulatory ReformThis is an update on China's recent regulatory reform from 2017. In the past 12 months, more draft regulations and guidelines have been finalised and gone into the implementation stage, which will change China's role in global drug development. Therefore, it is important to follow up to those changes, in order to fully explore China drug development potential.WEBCHINA2
Webinar: Get the Recognition You Deserve With CSciHave you been working in regulatory affairs for 4-6 years? Do you have a high level of competence? If so, then get the recognition you deserve with Chartered Scientist! Find out how from this webinar.WEBCSCI19
Webinar: Introduction To Data VisualisationThis webinar will provide an introduction to the latest data visualisation techniques being used to get the most insight from scientific and clinical data. How you visualise scientific and clinical data can powerfully influence the insights gained, conclusions drawn and the decisions that are made. This webinar can help you make the most of your data and ensure you aren’t missing important insights that could be used to support your internal decision making processes or your regulatory approvals.WEBDATA19
Webinar: Regulation of Medical Devices in the MENA RegionUnderstand the national requirements that must be met for approval of a medical device in the Middle East and North Africa (MENA) region. Look ahead to the impact of the MDR on approvals for medical devices in the region.WEBDEVMENA
Webinar: Feed Additive EfficacyThe regulatory framework and data required to establish the characterisation, quality, safety and efficacy of the different types of feed additives will be looked at during this webinar.WEBFEED18
Webinar: Food Supplements in RussiaAn overview of the regulation of food supplements in Russia.WEBFOODRUS
The Regulatory Environment in Australia and New ZealandGet an overview on the regulatory framework for medicines and processes in Australia and New Zealand, including expedited pathways.WEBGDAU
Webinar: GMDN Primer for Regulatory Affairs ProfessionalsGet an understanding of Global Medicinal Device Nomenclature (GMDN) and how this can be best managed.WEBGMDN19
Webinar: European Regulation of Herbal Medicinal ProductsThis webinar will provide delegates with an understanding of what is meant by a herbal medicine and will focus on the different regulatory routes by which herbal medicinal products can be licensed in Europe.WEBHERBAL
Webinar: Introduction To Health Technology Assessment (HTA)This webinar serves as introduction to the two day TOPRA CRED Workshop: ‘Health Technology Assessment as part of Regulatory Strategy?’WEBHTA16
Webinar: Identification of Medicinal Product LandscapeThis presentation will provide case studies representing EU and US environments and the experiences in preparing for IDMP followed up by with an IDMP Regulatory update.WEBIDMP17
Your Career in Regulatory Affairs: Your First StepsThis webinar recording will provide you with the key information that you will need to begin your career in regulatory affairs.WEBINTRO
Authoring of Generic Drug Product Labelling in the EU and USInterested in the latest generic drug product labelling requirements in the EU and US? Join our webinar to find out more!WEBLABEL
Webinar: EU Labelling RequirementsThis webinar will look at the steps involved in the EMA’s Linguistic Review procedure of product information following MA or post-authorisation procedures for centrally authorised products and how to efficiently manage the process.WEBLABEL19
Webinar: Lifecycle Management - Key International MarketsThis webinar will discuss key international markets such as, Brazil, Mexico, Korea, Taiwan, India, Australia/New Zealand, South Africa, Gulf Council and RussiaWEBLMKIM


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