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

Risk Management for Clinical Research Training Course

Risk Management for Clinical Research

4 Feb 2025 - Online webinar
Also on: 6 Jun 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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Advanced Project Management in Clinical Research Training Course

Advanced Project Management in Clinical Research

11 Feb 2025 - Online webinar
Also on: 9 Jun 2025

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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Application of Artificial Intelligence (AI) and Machine Learning in Clinical Trial Data Management Training Course

Application of Artificial Intelligence (AI) and Machine Learning in Clinical Trial Data Management

10 Mar 2025 - Online webinar
Also on: 30 Jun 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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Building Better Health via Digitalised and Personalised Patient Support Programmes Training Course

Building Better Health via Digitalised and Personalised Patient Support Programmes

12 Mar 2025 - Online webinar
Also on: 2 Jul 2025

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

Presented by Graham Howieson (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

22 Jan 2025 - Online webinar
Also on: 13 May 2025

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

31 Mar-3 Apr 2025 - Online webinar
Also on: 21 Jul 2025

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

Presented by Janette Benaddi (bio)

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Clinical Quality Management Systems Training Course

Clinical Quality Management Systems

23-24 Jan 2025 - Online webinar
Also on: 22 May 2025

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

29-31 Jan 2025 - Online webinar
Also on: 11 Jun 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

28-29 Apr 2025 - Online webinar
Also on: 21 Jul 2025

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

20-21 Jan 2025 - Online webinar
Also on: 8 May 2025

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

19 Mar 2025 - Online webinar
Also on: 17 Sep 2025

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

7 Apr 2025 - Online webinar
Also on: 14 Jul 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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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 Feb 2025 - Online webinar
Also on: 2 Jun 2025

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

14 Mar 2025 - Online webinar
Also on: 1 Jul 2025

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.

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

6-7 Feb 2025 - Online webinar
Also on: 23 Jun 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

17-18 Mar 2025 - Online webinar
Also on: 9 Jul 2025

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

Presented by Janette Benaddi (bio)

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

Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

7-8 May 2025 - Online webinar
Also on: 15 Sep 2025

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

Presented by Janette Benaddi (bio)

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Metrics and Earned Value in Clinical Research Projects Training Course

Metrics and Earned Value in Clinical Research Projects

5 Mar 2025 - Online webinar
Also on: 22 Jul 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

27 Feb 2025 - Online webinar
Also on: 4 Jun 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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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 The Pharmaceutical Market Training Course

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

26 Mar 2025 - Online webinar
Also on: 16 Jul 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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The Advancement of Research and Development (R&D) Clinical Trials using Software Automation Training Course

The Advancement of Research and Development (R&D) Clinical Trials using Software Automation

12 Feb 2025 - Online webinar
Also on: 4 Jun 2025

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

Presented by Graham Howieson (bio)

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The Importance of Patient Adherence Data and How Digital Tools Can Improve Patient Outcomes Training Course

The Importance of Patient Adherence Data and How Digital Tools Can Improve Patient Outcomes

26 Feb 2025 - Online webinar
Also on: 18 Jun 2025

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. 

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...

“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

“Great course, well spend money and time. ”

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

“As the person responsible of safety assessment and reporting in my department (clinical), I was hoping to strengthen my knowledge in this area. Especially when it comes to event assessment and classification.
This course helped me achieve that goal. [Speaker] is very knowledgeable on several topics.”

Stéphanie Trznadel, Clinical Trial Coordinator, SPINEART

“Fantastic, energetic, and positive. Very clear describing of the topics and good structure. Discussions. It made me feel more involved in the webinar. ”

Viktoriia Kyrylenko, Project Manager, BIOPHARMA PLASMA LLC

“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

“There were lots of useful links and information which I can use for further study of the risk management concepts and their application. ”

Vladilena Daly, Operations and Compliance Manager, CliebntPharma Ltd

“The speaker was knowledgeable, and made an effort to incorporate videos & discussions to break up a dry subject. ”

Beatrice Millward, Data Manager, Liverpool Clinical Trials Centre - University of Liverpool

“The overview was great, information clear and shared with links.”

Ana Karla Uribe Rivera, Research Fellow of Image Guided Surgery, IHU, Strasbourg

“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.