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Training courses & Webinars:
Regulatory Affairs
Our regulatory affairs training courses have been designed to update delegates on a wide range of regulatory topics, from updates on the latest regulations to registration procedures and strategies. We provide information on regulatory approval in key regions globally, with practical advice from our expert speaker panel.
Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products
5 Nov 2024 - Online webinar
Also on: 1 May 2025
Understanding the chemistry, manufacturing and controls (CMC) requirements for veterinary pharmaceuticals is essential to support successful registration in the EU.
A Practical Approach to Veterinary Vaccine Development and Registration in the EU
13-14 May 2025 - Online webinar
Also on: 6 Nov 2025
This event has been designed to give practical advice and guidance on how to successfully develop market approval in the EU. The programme will take participants through a step-by-step approach to the process and will also provide key guidance on how to maintain MA once achieved.
Presented by Mel Munro (bio)
A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China
2-3 Dec 2024 - Online webinar
Annual two-day regulatory update on animal feed and feed additives in the EU, USA and China.
Presented by
Bo Yang (bio)
and 5 more leading experts
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK
30 Apr 2025 - Online webinar
Also on: 21 Oct 2025
This course will provide an excellent opportunity to hear the latest developments from regulatory experts, and enable participants to discuss the implications of the regulations on working practices and the potential impact on future regulatory strategies.
Presented by
Theresa Jeary (bio)
and 4 more leading experts
Advanced Regulatory Affairs for Medical Devices
13-14 Feb 2025 - Online webinar
Also on: 3 Jun 2025
Planning your regulatory strategy to comply with the Medical Device Regulation (MDR)
An Essential Overview of Medical Information
29 Nov 2024 - Online webinar
Also on: 14 Mar 2025
In this one-day course, understand everything from the role of medical information to the guidelines for medical information and advertising.
Presented by Graeme Ladds (bio)
An Essential Overview of the Medical Device Industry
14 Mar 2025 - Online webinar
Also on: 3 Jul 2025
This one-day workshop aims to give all the key information necessary to understand the regulation of medical devices and diagnostics and to appreciate the key differences from pharmaceutical regulation.
An Essential Overview of the Pharmaceutical and Biotech Industries
16 Jan 2025 - Online webinar
Also on: 12 May 2025
This programme will give you an invaluable overview of the pharmaceutical industry, from discovery of the molecule through development to marketing.
Presented by Laura Brown (bio)
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices
11 Nov 2024 - Online webinar
Also on: 1 May 2025
Sterile devices are free of viable microorganisms and EO sterilization is one of the key processes in the production of sterile medical devices. This course provides an introduction to the regulatory requirements as they relate to EO sterilisation and how manufacturers may demonstrate compliance.
Presented by Annette Callaghan (bio)
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals
17 Mar 2025 - Online webinar
Also on: 9 Jul 2025
This course will cover the key regulations used globally in human factors and usability engineering: the specific standards and guidances, methods, and the tools commonly used in medical device development.
Presented by Greg Thay (bio)
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices
22 May 2025 - Online webinar
Also on: 17 Nov 2025
Sterile devices are free of viable microorganisms and the sterile barrier system is the key to maintaining this sterility until the medical device is ready to be used on a patient. This course provides an introduction to the regulatory requirements as they relate to typical sterile barrier systems used for single-use and reusable medical devices, and how manufacturers may demonstrate compliance.
Presented by Annette Callaghan (bio)
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices
13 Mar 2025 - Online webinar
Also on: 3 Jul 2025
This course has been specifically designed to provide an essential introduction to ISO 13485 and the QMS and provides a comprehensive and valuable overview of the requirements and responsibilities involved.
Where ever you and your company sit within the medical device arena this is an excellent opportunity to become appraised of the requirements.
Presented by Linda Garrod (bio)
An introduction to Risk Management ISO 14971:2019
11 Mar 2025 - Online webinar
Also on: 11 Jul 2025
Dive into the core principles of risk management using ISO14971:2019. Learn to assess, analyse, and mitigate risks effectively, ensuring compliance with international standards and enhancing decision-making in various industries.
Presented by Linda Garrod (bio)
An Introduction to the Medical Device Regulation
25-27 Mar 2025 - Online webinar
Also on: 16 Jul 2025
This seminar provides a detailed introduction to the European medical device legislation. It will explain the Regulation and which products are covered, the involvement of Notified Bodies, how to choose one and outline what a manufacturer must do.
Animal Feed and Feed Additive Registration in China and Thailand
27 Feb 2025 - Online webinar
Also on: 26 Jun 2025
Learn how to navigate the regulatory system for animal feed and feed additives in two emerging markets.
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions
9 Apr 2025 - Online webinar
Also on: 17 Sep 2025
This course will allow participants to explore the regulatory landscapes governing AMR, discover innovative solutions and understand the challenges AMR poses across different sectors.
Presented by Linda Oyama (bio)
Best Practice for Writing Effective SOPs
12 Dec 2024 - Online webinar
Also on: 27 Mar 2025
An essential course for ensuring compliance with regulatory requirements and including best practice SOP writing using process mapping.
Presented by Laura Brown (bio)
Biological Evaluation of Medical Devices
15-16 Jan 2025 - Online webinar
Also on: 15 May 2025
Key guidance on how to use the ISO 10993 series of standards and successfully apply a risk management approach to the biological evaluation of medical devices.
*Includes:* Interactive workshops and discussion sessions
Presented by Annette Callaghan (bio)
CAPA (Corrective and Preventative Action)
13 Dec 2024 - Online webinar
Also on: 28 Mar 2025
This course will cover CAPA methodology and documentation, diagnosing process improvement, developing options for process improvement, and planning and implementation in process improvements and CAPA.
Presented by Laura Brown (bio)
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products
27-28 Feb 2025 - Online webinar
Also on: 26 Jun 2025
The regulatory requirements for Biological drug products are complex, and pharmaceutical companies are continuously under pressure to ensure regulatory compliance from drug discovery to post-marketing surveillance.
This course has been designed to help you navigate the complex regulatory requirements for biological drugs, including ATMPs. It will clearly depict the differences between small and large molecules and the development approaches which reflect the type of molecule. It will address the key aspects of the CTD, look at the CMC regulatory requirements during different stages of development, and discuss the importance of change control.
Presented by Andrew Willis (bio)
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW)
28 Feb 2025 - Online webinar
Also on: 9 Jul 2025
Master the complexities of software classification under the Medical Device Regulations (MDR), ensuring compliance and clarity with expert insights into MDCG guidelines, practical case studies, and regulatory frameworks.
Presented by Koen Cobbaert (bio)
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
5-6 Feb 2025 - Online webinar
Also on: 18 Jun 2025
This seminar looks at the latest guidance on how to prepare a clinical overview and summary in accordance with regulatory expectations and to comply with the requirements of the Common Technical Document (CTD).
Presented by John Price (bio)
Cyber Security for Medical Devices
28-29 Jan 2025 - Online webinar
Also on: 8 May 2025
This seminar will provide you with an understanding of cybersecurity and its increasing regulatory focus, and how to embed and apply state-of-the-art security in your existing processes to deliver safe and secure products and solutions.
Presented by Ben Kokx (bio)
Data Innovation for AI-enabled Medical Devices
28 Feb 2025 - Online webinar
Also on: 9 Jul 2025
This course provides an in-depth understanding of data governance for AI-enabled medical devices, focusing on European regulations like the AI Act and GDPR, ensuring compliance while fostering innovation in high-risk AI systems.
Presented by Koen Cobbaert (bio)
Deep Dive into the IVDR Annex XIII
5 Mar 2025 - Online webinar
Also on: 10 Jul 2025
Explore IVDR Annex XIII in-depth, covering Performance Evaluation, Performance Studies, and Post-market Performance. Learn what information is required, where to put it, and when, with a detailed review of nine essential documents.
Presented by Jane Leadsham (bio)
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW)
3 Mar 2025 - Online webinar
Also on: 10 Jul 2025
Gain essential knowledge in developing and managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW), focusing on regulatory compliance, risk management, and lifecycle management to ensure safety and effectiveness.
Presented by Koen Cobbaert (bio)
EU Pharmaceutical Regulations & Strategy
10-11 Feb 2025 - Online webinar
Also on: 9 Jun 2025
The course will provide an up-to-date overview of the current European pharmaceutical regulatory environment including procedures for obtaining marketing authorisation and post-approval obligations. The proposed changes to the EU pharmaceuticals legislation will be discussed in the relevant sections and impact on strategic considerations for obtaining and maintaining marketing authorisations Procedures for obtaining marketing authorisations in in the UK will be discussed.
Presented by Norah Lightowler (bio)
EU Proposed Pharmaceutical Legislation Changes
20 Jan 2025 - Online webinar
Also on: 19 May 2025
This course will provide an up-to-date overview of current European pharmaceutical legislation and the regulatory impact of the proposed changes.
Presented by Norah Lightowler (bio)
FDA Approval Process for Medical Devices
2-3 Dec 2024 - Online webinar
Also on: 31 Mar 2025
This seminar will provide a solid foundation in the approval and clearance processes for medical devices in the United States including the underlying legal and regulatory requirements and the 'general controls' applicable to all devices.
Presented by Jonathan Hughes (bio)
Global Pharmaceutical Regulatory Affairs Summer School
9-13 Jun 2025 - Online webinar
Unlock the world of pharmaceutical regulatory excellence with our Global Pharmaceutical Regulatory Affairs training – an intensive journey through the diverse regions, offering practical insights, expert guidance, and strategic mastery for professionals seeking to navigate and succeed in the dynamic global regulatory landscape.
Presented by
Alan Chalmers (bio)
and 8 more leading experts
Human Factors and Usability Engineering in the Development of Drug Delivery Products
5-6 Dec 2024 - Online webinar
Also on: 15 Jan 2025
This two-day workshop has been designed specifically for product developers who want to incorporate human factors testing into their product development, or need to provide the regulators with specific usability data for their device.
Presented by Richard Featherstone (bio)
ICH Q9(R1) Quality Risk Management (QRM)
29 Jan 2025 - Online webinar
Also on: 12 May 2025
ICH Q9(R1) Quality Risk Management has recently been updated by the regulators. This training course will bring participants right up-to-date with the latest Q9(R1) requirements. It will explain the changes and give context as to how these impact pharmaceutical products and processes. It will cover a range of product types and situations.
Presented by Bruce Davis (bio)
Introduction to the In-Vitro Diagnostic Regulation (IVDR)
5-6 Feb 2025 - Online webinar
Also on: 16 Jul 2025
This two-day seminar will clarify the requirements applicable to in-vitro diagnostic devices under the IVD Regulation (EU) 2017/746. It will highlight the major changes to responsibility and product data expectations and will review the impact to industry.
Presented by Stuart Angell (bio)
Introduction to the New Performance Evaluation Requirements Mandated Under the IVDR (2017/746)
4 Mar 2025 - Online webinar
Also on: 9 Jul 2025
Understand the essentials of performance evaluation under the In Vitro Diagnostic Regulation (2017/746) in this comprehensive seminar. Essential for regulatory compliance and business success.
Presented by Jane Leadsham (bio)
Managing Competence within the Medical Device Industry
26 Mar 2025 - Online webinar
Also on: 11 Jul 2025
This webinar has been designed to help you understand the ‘big picture’ of competence management, from selection of the right competencies for success to the maintenance of collective organisational knowledge.
Presented by Anne Jury (bio)
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW)
26-27 Feb 2025 - Online webinar
Also on: 7 Jul 2025
Learn the critical regulatory requirments and best practices for obtaining market authorisation or Software as a Medical Device (SaMD) and Medical Device Software (MDSW) in global markets.
Presented by Koen Cobbaert (bio)
Masterclass: Market Authorisation of AI-enabled Medical Devices
4 Apr 2025 - Online webinar
Also on: 11 Jul 2025
This course provides essential guidance on navigating regulatory requirements and securing market authorization for AI-based medical devices, covering key regulations, compliance strategies, and best practices for global market access.
Presented by Koen Cobbaert (bio)
Medical Device Regulation in the Eurasian Union, Russia and the CIS
9-10 Dec 2024 - Online webinar
Also on: 3 Apr 2025
A comprehensive overview of medical device regulatory affairs in Russia and the Eurasian Union. Key countries covered include Armenia, Azerbaijan, Belarus, Georgia, Kazakhstan, Kyrgyzstan, Moldova, Russia, Tajikistan, Turkmenistan and Ukraine.
Presented by Anna Harrington-Morozova (bio)
Medical Device Regulations in the Middle East and North Africa
10-11 Mar 2025 - Online webinar
Also on: 23 Jul 2025
This seminar will provide an essential overview of the key areas of requirements for product approvals for medical devices in the Middle East and North Africa. Covering Algeria, Bahrain, Egypt, Israel, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, Palestine, Saudi Arabia, Sudan, Syria, Tunisia, UAE and Yemen.
Medical Device Single Audit Programme (MDSAP)
28-29 Nov 2024 - Online webinar
Also on: 24 Mar 2025
The Medical Device Single Audit Program (MDSAP) was developed by the International Medical Device Regulators Forum (IMDRF) to conduct regulatory audits of the quality management systems (QMS) used by manufacturers of medical devices.
This course will prepare you to host a MDSAP audit within your organisation, and allow you to determine if your own internal QMS processes are consistent with requirements of the MDSAP for the jurisdictions where your products are marketed, or for those markets which you are planning to access.
Presented by Stuart Angell (bio)
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
18-21 Nov 2024 - Online webinar
An introduction to medical device software regulations and requirements to include the latest EU and FDA guidance and risk management.
Navigating China’s API Regulations: An Essential Guide to DMF Registration
12 Feb 2025 - Online webinar
Also on: 23 Jun 2025
Enhance your knowledge of the regulatory requirements for Active Pharmaceutical Ingredients and the Drug Master File in China. An opportunity to learn the quickest pathway options for DMF registration and to hear from industry leaders in this important region.
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products
21-22 Jan 2025 - Online webinar
Also on: 19 May 2025
Gain practical guidance on the complex regulatory landscapes of EU and FDA for drug/device & device/drug combination products in this comprehensive course.
Presented by
Tina Amini (bio)
and 3 more leading experts
Navigating Regulatory Compliance Whilst Developing and Distributing PCR-Based IVD Tests
6 Mar 2025 - Online webinar
Also on: 26 Jun 2025
In this three-hour course, learn from an expert about developing and distributing PCR-based IVD tests, as well as exploring the latest regulatory requirements.
Presented by Dmitriy Kosarikov (bio)
Non-Conformance and Corrective Action for Medical Device Manufacturers
12 Dec 2024 - Online webinar
Also on: 10 Apr 2025
The identification of non-conformances and ensuring that they are dealt with in a timely and appropriate manner is a key part of any medical device Quality Management System (QMS). This course provides an introduction to the regulatory requirements as they relate to the identification and handling of non-conformances and how manufacturers may demonstrate compliance.
Presented by Annette Callaghan (bio)
Pharmaceutical Regulatory Affairs in Africa
19-20 Nov 2024 - Online webinar
Also on: 24 Feb 2025
Covering the key regions of South Africa, Namibia, Zimbabwe, Zambia, Malawi, Tanzania, Kenya, Uganda, Nigeria, Ghana and Maghreb countries - Algeria, Morocco, Tunisia
Pharmaceutical Regulatory Affairs in Asia
25-27 Feb 2025 - Online webinar
Also on: 11 Jun 2025
This seminar will provide an overview of the key areas of pharmaceutical regulatory affairs in Asia including, China, Hong Kong SAR, Brunei, the Philippines, India, Indonesia, Malaysia, Singapore, Thailand, Cambodia, Laos, Vietnam, Taiwan, Korea, Japan
Pharmaceutical Regulatory Affairs in China
10-11 Dec 2024 - Online webinar
Also on: 31 Mar 2025
A detailed overview of the key areas of pharmaceutical regulatory affairs in China, Hong Kong, Macau and Taiwan.
Pharmaceutical Regulatory Affairs in Latin America
25 Feb 2025 - Online webinar
Also on: 18 Jun 2025
This programme offers a detailed examination of the regulatory landscape, emphasizing both challenges and opportunities for the pharmaceutical industry across key Latin American markets, including Argentina, Brazil, Chile, Colombia, Mexico, and Peru.
Presented by Belkys Ruiz (bio)
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union
6-7 Feb 2025 - Online webinar
Also on: 19 Jun 2025
This interactive course will discuss the regulatory requirements within these regions, and discuss the implications of the new joint Eurasian Union regulation.
Presented by Anna Harrington-Morozova (bio)
Pharmaceutical Regulatory Affairs in the Middle East
9-10 Dec 2024 - Online webinar
Also on: 25 Feb 2025
Covering Bahrain, Egypt, Iran, Iraq, Israel, Jordan, Kuwait, Lebanon, Libya, Oman, Palestine, Qatar, Saudi Arabia, Sudan, Syria, UAE and Yemen
Post-Market Surveillance - Practical Application for Medical Devices and IVDs
12 Feb 2025 - Online webinar
Also on: 5 Jun 2025
In this practical, one-day course, learn the regulatory requirements needed for successful post-market surveillance of medical devices and IVDs.
Practical Implementation of a Human Factors Study
4-5 Mar 2025 - Online webinar
Also on: 1 Jul 2025
This training focuses on the practical and logistical aspects of planning, preparing and performing human factors studies for medical devices and combination products.
Presented by Richard Featherstone (bio)
Registration of Veterinary Pharmaceuticals in China
27 Feb 2025 - Online webinar
Also on: 26 Jun 2025
Learn how to navigate the regulatory system of veterinary pharmaceuticals in China.
Presented by Bi Jun (bio)
Regulatory Affairs for Support Staff
27-28 Jan 2025 - Online webinar
Also on: 12 May 2025
This two-day course provides an introduction to pharmaceutical regulatory affairs and the basics of drug development and has been designed specifically for those working in a support staff role.
Presented by Norah Lightowler (bio)
Regulatory Strategies for Orphan Drugs
10 Feb 2025 - Online webinar
Also on: 23 Jun 2025
This must-attend event will provide an essential overview of the opportunities and challenges presented by orphan drug regulation.
Presented by Shaun Stapleton (bio)
Risk Management for Pharma and Biopharma Professionals
4 Feb 2025 - Online webinar
Also on: 6 Jun 2025
This essential course will explain the importance of using risk management techniques in drug and device development to comply with the latest focus on inspection in this area.
Presented by Laura Brown (bio)
Sterilization of Medical Devices
3-4 Feb 2025 - Online webinar
Also on: 5 Jun 2025
Sterile devices are free of viable microorganisms and sterilization is one of the key processes in the production of sterile medical devices. Regulations for medical devices include particular requirements for devices supplied or intended to be used in a sterile state. These regulatory requirements relate to general safety and performance aspects for the products, and the requirements for independent, third-party conformity assessment of the processes for achieving sterility. Evidence of successful sterilization is important and expected when demonstrating conformity with the regulations. This course provides a comprehensive overview of these regulatory requirements and how to comply, together with the science and standards that support them.
Presented by Annette Callaghan (bio)
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA
16-19 Jun 2025 - London
This practical four-day course provides a comprehensive understanding of veterinary medicine development in the EU and USA.
The Common Technical Document (CTD) Submission in the MENA Region
28 Nov 2024 - Online webinar
Also on: 13 Mar 2025
This one-day course will provide you with an in depth understanding of the technical and regulatory requirements of CTD submissions in different countries in the MENA region.
Presented by Mohammad Fat'hy Elnadi (bio)
The FDA Drug Approval Process
2-3 Dec 2024 - Online webinar
Also on: 24 Feb 2025
A comprehensive overview of FDA procedures, requirements for marketing authorisations and recent developments affecting the drug approval process in the US
Presented by Andrew Willis (bio)
The Medical Device School - From Concept to CE Marking
2-6 Dec 2024 - Online webinar
Also on: 9 Jun 2025
This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process.
Presented by
Stuart Angell (bio)
and 7 more leading experts
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry
13-14 Jan 2025 - Online webinar
Also on: 12 May 2025
In this webinar, we will discuss the major requirements and strategies on Nitrosamines, a hot topic that is on the forefront of many company's minds.
Presented by Jason Brown (bio)
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR
23 Jan 2025 - Online webinar
Also on: 22 May 2025
This one day course will cover the role of the Person Responsible for Regulatory Compliance (PRRC) introduced by the implementation of the Medical Device Regulation 2017/745 and the In-Vitro Diagnostic Device Regulation 2017/746. The course will review Article 15 from the regulation in detail to enable understanding of the intent of each requirement. It will also present the UK Medical Device Regulation requirements and discuss the proposed Qualified Person role with current information.
Presented by Stuart Angell (bio)
UK Conformity Assessed (UKCA) Marking for Medical Devices
10 Feb 2025 - Online webinar
Also on: 26 Jun 2025
This course provides UK and global companies practical guidance on what you need to do to continue market access or gain market access with your medical device in the UK.
Presented by Janette Benaddi (bio)
Understanding Active Pharmaceutical Ingredients (APIs)
25-26 Mar 2025 - Online webinar
Also on: 16 Jul 2025
This course will cover key terminology, the EU and USA regulatory framework, Good Manufacturing Practice (GMP) requirements including controls and validation, and consider Good Distribution Practice (GDP) and how to manage your supply chain.
Presented by Paul Palmer (bio)
Understanding Computer System Validation (CSV)
18-19 Mar 2025 - Online webinar
Also on: 9 Jul 2025
This course covers the key concepts of computer systems validation and provides practical guidance on how to comply with the regulations applicable to the pharmaceutical industry.
Presented by Paul Palmer (bio)
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers
5 Dec 2024 - Online webinar
Also on: 24 Mar 2025
The information supplied with medical devices, both on their labels and in any accompanying Instructions for Use form part of the device itself, and are critical to the safety and performance of the device and to compliance with regulatory requirements. This course provides an introduction to the regulatory requirements as they relate to the labelling of medical devices and how manufacturers may demonstrate compliance.
Presented by Annette Callaghan (bio)
US FDA - Understanding Key Factors When Working with the FDA
27 Nov 2024 - Online webinar
Also on: 13 Mar 2025
This course has been designed to provide an essential overview of the critical factors when working with the FDA (Food and Drug Administration). For those short on time this course is for you, as you will receive a focused and comprehensive overview of the key strategic considerations when making applications to the FDA.
Presented by Andrew Willis (bio)
Variations to Marketing Authorisations
28-29 Nov 2024 - Online webinar
Also on: 6 Feb 2025
A two-day event that will provide an invaluable overview of the EU system for variations, with practical advice on the preparation and submission of variation applications using the various European procedures.
Presented by Andrew Willis (bio)
Veterinary Pharmaceutical Submissions in the EU
26-27 Nov 2024 - London
Also on: 19 May 2025
Presentations will cover the regulatory framework, pharmaceutical, toxicological and pharmacological data, safety risk assessments, pre-clinical and clinical data, critical expert reports and regulatory submissions.