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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
30/11/2020An Introduction To Pharmacovigilance for RA ProfessionalsThis webinar will explore the integrated environment between pharmacovigilance and regulatory affairs, focusing on the basics of signal management process and medical writing requirements.WEBPHV
08/12/2020An Overview of the Brazilian Medical Device RegulationsThis webinar will outline the regulatory environment for medical devices and the basic processes for notification and registration in Brazil.WEBMDBR


Member webinars *

Start dateTitleDescription
08/12/2020TOPRA In Sweden - Clinical Trials (FIH Studies)TOPRA In Sweden present a webinar on Clinical Trials. This evening is an excellent opportunity to discuss early clinical trials of medicinal products, First-in-Human (FIH) studies.SWEDEC2020
18/12/2020TOPRA In India - Brexit WebinarThis TOPRA In India sponsored webinar will explore the latest information & related guidance around Brexit for pharmaceutical companies.INDDEC2020

* 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

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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
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: Regulatory 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
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
Understanding the Needs of HTA as a Market Access ToolThis webinar will cover key HTA considerations in the UK and EU for regulatory professionals planning their regulatory strategy for non-drug technologies.WEBHTA
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


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