IPI Academy’s clinical training courses cover all aspects of clinical research including regulatory requirements, the conduct of trials, human factors and data management. Our expert speakers will cover the latest regulatory updates and key topics relevant for all clinical trial professionals.
Our courses provide a comprehensive portfolio of all aspects of clinical research for pharmaceuticals, medical devices and veterinary medicines and provide an excellent opportunity to understand the complexities and requirements involved in this critical area and learn from leading experts in this field.
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This essential course will explain the importance of using risk management techniques in clinical trials to comply with the latest focus on inspection in this area.
New for 2025
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This Clinical Research Project Management Training course will provide you with key techniques to apply during your clinical research project to aid successful project delivery. This course will be key for those involved in clinical research projects and will cover system thinking, agile approaches and risk analysis.
New for 2025
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This course will help delegates gain a better understanding of the automation technology driving change within the clinical trials landscape.
New for 2025
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AI and Machine Learning are revolutionising clinical trial data management by enhancing efficiency, streamlining processes, and minimising human error. This course will be of use in both the pharmaceutical and medical device industry.
New for 2025
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Learn how to build digital technology that is specifically aligned to match with the patient, the study, the disease and the treatment program.
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This one-day course will provide a clear understanding of the clinical evaluation requirements and their practical application for software products, including AI/ML-based devices.
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Cover all the aspects of clinical evaluation in line with the European medical device regulations and applicable guidance documents
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A two-day course that will ensure you comply with new regulatory requirements.
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The leading clinical research project management course designed specifically for the pharma/bio industries – also applicable to those working in medical devices and animal health
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This course will assure monitors understand the importance of compliance with latest ICH GCP R3 requirements, and how these apply to monitoring clinical trials in the future.
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This course will take you through the key regulatory and guideline requirements for clinical research in Europe, including the new EU Clinical Trial Regulation and a brief review of key FDA requirements.
New for 2025
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An excellent opportunity to hear from two renowned cognition experts and gain a better understanding on the selection and successful integration of cognitive testing into therapeutic development programmes, as well as the emerging science of blood-based biomarkers.
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Data integrity is a critical issue in document governance and is increasingly becoming a focus for regulatory inspections globally. This course will equip you with the necessary knowledge to identify and avoid potential data integrity issues before auditors do.
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This course will provide an update on the experience of working to the regulation since Go-live, to help your implementation and compliance including transferring clinical trials from the directive to the regulation.
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This course provides recent updates on the New ICH GCP R3 guideline, EU Clinical Trial Regulation update, other EU and FDA requirements, consideration for managing studies in the future and AI and other technology developments.
New for 2025
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In this course, you will determine the value of remote patient adherence monitoring and learn how to stay ahead of the curve by creating your own digital solutions.
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Optimising oversight for inspection compliance.
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Gathering and using clinical evidence for CE marking and post-market compliance in line with the new MDR.
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An essential overview of medical device clinical evaluations, clinical investigations, post-market clinical follow-up requirements and adverse event and vigilance reporting.
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This workshop will focus on the effective use of metrics to monitor the real progress of your clinical research project. A valuable master class for anyone involved in clinical research.
New for 2025
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Explore the microbiome and its high clinical relevance, as well as learning about the different methodology used in microbiomic clinical trials.
Live online, Classroom
This seminar will take many aspects of animal health and veterinary research and development through a typical clinical trial, and pay attention to compliance with Good Clinical Practice (GCP) as outlined in the two guidelines on safety and efficacy produced by FEDESA and the CVMP.
New for 2025
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A deep dive into the importance of real world evidence (RWE), real world data (RWD) and artificial intelligence (AI) in pharmaceuticals.
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