- Home
- Life Sciences
- Clinical Research
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
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)
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)
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)
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)
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)
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)
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)
Clinical Trial Monitoring
2-3 Dec 2024 - Online webinar
Also on: 28 Apr 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)
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)
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.
Data Integrity and Document Management
6 Dec 2024 - Online webinar
Also on: 7 Apr 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)
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)
GCP and Clinical Research Update - Hot Inspection Topics
22 Nov 2024 - Online webinar
Also on: 14 Mar 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)
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)
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)
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
15-16 Jan 2025 - Online webinar
Also on: 7 May 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)
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)
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)
Practical Implementation of GCP in Veterinary Field Studies
26-27 Nov 2024 - London
Also on: 14 May 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.
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)
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)
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)