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
29-30 Nov 2023 - Online webinar
Also on: 26 Feb 2024
Cover all the aspects of clinical evaluation in line with the European medical device regulations and applicable guidance documents
25-26 Jan 2024 - Online webinar
Also on: 23 May 2024
A two-day course that will ensure you comply with new regulatory requirements.
Presented by Laura Brown (bio)
16 Feb 2024 - Online webinar
Also on: 10 Jun 2024
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)
26-28 Feb 2024 - Online webinar
Also on: 26 Jun 2024
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)
29-30 Apr 2024 - Online webinar
Also on: 11 Jul 2024
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)
22-23 Jan 2024 - Online webinar
Also on: 2 May 2024
This course will take you through the key regulatory and guideline requirements for clinical research in Europe, including the new EU Clinical Trial Regulation one year on and a brief review of key FDA requirements.
Presented by Laura Brown (bio)
20 Mar 2024 - Online webinar
Also on: 18 Sep 2024
An an excellent opportunity to hear from a renowned cognition expert and gain a better understanding on the selection and successful integration of cognitive testing into therapeutic development programmes.
Presented by John E. Harrison (bio)
12 Apr 2024 - Online webinar
Also on: 22 Jul 2024
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)
15-16 Feb 2024 - Online webinar
Also on: 20 May 2024
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)
15 Mar 2024 - Online webinar
Also on: 1 Jul 2024
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)
15-16 Jan 2024 - Online webinar
Also on: 18 Apr 2024
Optimising oversight for inspection compliance
Presented by Laura Brown (bio)
18-21 Mar 2024 - Online webinar
Also on: 10 Jul 2024
Gathering and using clinical evidence for CE marking and post-market compliance in line with the new MDR
Presented by Janette Benaddi (bio)
17-18 Jan 2024 - Online webinar
Also on: 21 May 2024
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)
6 Mar 2024 - Online webinar
Also on: 11 Jul 2024
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)
19-20 Mar 2024 - Online webinar
Also on: 26 Nov 2024
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.