Training courses & Webinars:
Clinical Research

Management Forum’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. 

 

 

 

Please note: full product details will be shown on our training portal IPI Academy where you can find out more and book

Advanced Project Management in Clinical Research Training Course

Advanced Project Management in Clinical Research

3 Oct 2025 - Online webinar

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.

Presented by Roger Joby (bio)

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AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Training Course

AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects

30 Jun 2025 - Online webinar
Also on: 6 Nov 2025

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.

Presented by Zuzanna Kwade (bio)

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Clinical Evaluation of Medical Device Software and Software as a Medical Device Training Course

Clinical Evaluation of Medical Device Software and Software as a Medical Device

1 Oct 2025 - Online webinar

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.

Presented by Zuzanna Kwade (bio)

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Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Training Course

Clinical Evaluation of Medical Devices: The Clinical Evaluation Report

21-22 Jul 2025 - Online webinar
Also on: 25 Nov 2025

Cover all the aspects of clinical evaluation in line with the European medical device regulations and applicable guidance documents

Clinical Quality Management Systems Training Course

Clinical Quality Management Systems

18-19 Sep 2025 - Online webinar

A two-day course that will ensure you comply with new regulatory requirements.

Presented by Laura Brown (bio)

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Clinical Research Project Management Training Course

Clinical Research Project Management

11-13 Jun 2025 - Online webinar
Also on: 22 Oct 2025

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

Presented by Laura Brown (bio)

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Clinical Trial Monitoring Training Course

Clinical Trial Monitoring

21-22 Jul 2025 - Online webinar

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.

Presented by Laura Brown (bio)

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Clinical Trial Regulatory Requirements Training Course

Clinical Trial Regulatory Requirements

15-16 Sep 2025 - Online webinar

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.

Presented by Laura Brown (bio)

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Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration Training Course

Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration

17 Sep 2025 - Online webinar

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.

Presented by John E. Harrison (bio)
Alison Green (bio)

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Data Integrity and Document Management Training Course

Data Integrity and Document Management

14 Jul 2025 - Online webinar
Also on: 11 Dec 2025

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.

Presented by Laura Brown (bio)

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Digital Technology and Personalisation in Patient Support Programmes Training Course

Digital Technology and Personalisation in Patient Support Programmes

2 Jul 2025 - Online webinar
Also on: 5 Nov 2025

Learn how to build digital technology that is specifically aligned to match with the patient, the clinical study, the disease and the treatment programme.

Presented by Graham Howieson (bio)

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EU (European Union) Clinical Trial Regulation 536/2014: Overview and Implementation Experience Training Course

EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience

13-14 Oct 2025 - Online webinar

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.

Presented by Laura Brown (bio)

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GCP (Good Clinical Practice) and Clinical Research Update - Hot Inspection Topics Training Course

GCP and Clinical Research Update - Hot Inspection Topics

7 Jul 2025 - Online webinar
Also on: 21 Nov 2025

This course provides the latest updates on the finalised ICH GCP E6 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.

Presented by Laura Brown (bio)

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Managing Service Providers including CRO (Contract Research Organisation) and CMOs oversight to comply with ICH GCP (Good Clinical Practice) R3 Training Course

Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3

23-24 Jun 2025 - Online webinar
Also on: 16 Oct 2025

Optimising oversight for inspection compliance.

Presented by Laura Brown (bio)

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Medical Device Studies: Clinical Evidence Training Course

Medical Device Studies: Clinical Evidence

15-16 Oct 2025 - Online webinar

Gathering and using clinical evidence for CE marking and post-market compliance in line with the new MDR.

Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course

Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

15-16 Sep 2025 - Online webinar

An essential overview of medical device clinical evaluations, clinical investigations, post-market clinical follow-up requirements and adverse event and vigilance reporting.

Metrics and Earned Value in Clinical Research Projects Training Course

Metrics and Earned Value in Clinical Research Projects

22 Jul 2025 - Online webinar
Also on: 24 Nov 2025

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.

Presented by Roger Joby (bio)

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Microbiomics in Clinical Trials Training Course

Microbiomics in Clinical Trials

4 Jun 2025 - Online webinar
Also on: 14 Oct 2025

Explore the microbiome and its high clinical relevance, as well as learning about the different methodology used in microbiomic clinical trials.

Presented by Nikolaj Sørensen (bio)

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Navigating ICH GCP (Good Clinical Practice) E6 (R3): What You Need to Know Training Course

Navigating ICH GCP E6 (R3): What You Need to Know

12 Sep 2025 - Online webinar
Also on: 15 Jan 2026

This brand new course on the recently published and long-awaited ICH GCP E6 (R3) is designed to help participants stay compliant and implement the new guideline effectively.

Presented by Laura Brown (bio)

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Practical Implementation of GCP (Good Clinical Practice) in Veterinary Field Studies Training Course

Practical Implementation of GCP in Veterinary Field Studies

14-15 May 2025 - Online webinar
Also on: 25 Nov 2025

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.

Presented by Rachel Anderson (bio)
Donna Taylor (bio)
Jenny Webster (bio)

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Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma Training Course

Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma

16 Jul 2025 - Online webinar
Also on: 19 Nov 2025

A deep dive into the importance of real world evidence (RWE), real world data (RWD) and artificial intelligence (AI) in pharmaceuticals.

Presented by Graham Howieson (bio)

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Risk Management for Clinical Research Training Course

Risk Management for Clinical Research

6 Jun 2025 - Online webinar
Also on: 7 Oct 2025

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.

Presented by Laura Brown (bio)

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Software Automation in Research and Development (R&D) Clinical Trials Training Course

Software Automation in Research and Development (R&D) Clinical Trials

1 Oct 2025 - Online webinar

This course will help delegates gain a better understanding of the software automation technology driving change within the clinical trials landscape.

Presented by Graham Howieson (bio)

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Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes Training Course

Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes

18 Jun 2025 - Online webinar
Also on: 15 Oct 2025

In this course, you will see the value of remote patient adherence monitoring and learn how to stay ahead of the curve by creating your own digital solutions. 

Presented by Graham Howieson (bio)

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In-house training

We can provide any of our courses on an in-house basis - at your location or online, with a programme and presenters tailored to your exact requirements. If you require training for multiple staff members, contact us to see how we can work with you.

Previous attendees said...

“Great course, well spend money and time. ”

Suada Pieper, Associate Specialist, clinical research, MSD Animal Health Innovation

“The content was very thorough, the presentations were held in an encouraging way and the speakers had impressive knowledge of their area and were very helpful. All [their].presentations were very valuable.”

Bernadett Riszne Ladanyi, QA Specialist/Auditor, Ceva-Phylaxia

“This was a very well-structured course that can be useful also to people working many years in GCP studies. The content was very interesting and helpful and allowed interaction and questions during the seminar. The excellent speakers are experienced and tried to facilitate all questions raised during the presentations. ”

Eleni Vatzia, Clinical Research Manager, MSD Animal Health

“It was very useful to have specific ideas, tools, websites and portals introduced as to what should be done for CRO oversight.”

Kenji Tada, Unit Manager, Clinical Operation Unit, JCR Pharmaceuticals Co

“Very insighful training, interactive and lively session with interesting content. small participating group, really appreciated it! [sic]”

Dalila Arbadji, Senior Clinical Trial Administrator, Chiesi

“I was hoping to get knowledge on how to manage clinical trial as a legal counsel in a pharmaceutical company. The speaker was clear [and] I lear[n]t a lot but more about regulatory aspect.”

Salome Hamon, Junior Legal Counsel, Curium Holding France SAS

“The content of training materials covered all the expected regulatory topics. [Speaker] made a great speech and answered clearly to the questions raised. Workshops sessions were useful to practice.”

Marieme Ndeye Gueye , Senior CTA, Chiesi France

“It was a really nice 2 day course. Good variety between information and workshops and the practical tips were usefull. The enthusiasm of the trainers was really nice as well.”

Tamara Giesen, Quality Assurance Officer, Royal GD

“I got some valuable tips during [this] course.”

Zonera Hassan, Project Manager, CHEPLAPHARM Arzneimittel GmbH

“Overall the webinar was well-presented, the content provided was very detailed and the speaker [k]new the topic well.”

Davinia-Ann Cardona, Quality Associate, Orphalan Ltd.