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In-house & bespoke training:
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
In-house & bespoke training
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.
Typically presented by Roger Joby (bio)
| Delivery: collaborative classroom |
Clinical Evaluation of Medical Device Software
In-house & bespoke training
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.
Typically presented by Zuzanna Kwade (bio)
| Delivery: collaborative classroom |
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
In-house & bespoke training
Cover all the aspects of clinical evaluation in line with the European medical device regulations and applicable guidance documents
Rated by attendees to the public programme
Typically presented by Janette Benaddi (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |
Clinical Quality Management Systems
In-house & bespoke training
A two-day course that will ensure you comply with new regulatory requirements.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |
Clinical Research Project Management
In-house & bespoke training
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
Typically presented by Laura Brown (bio)
| Typical duration: 3 days | |
| Pricing from £1,200 per attendee | |
| Delivery: collaborative classroom |
Clinical Trial Monitoring
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Delivery: collaborative classroom |
Clinical Trial Regulatory Requirements
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |
Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration
In-house & bespoke training
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.
Typically presented by John E. Harrison (bio) , Alison Green (bio)
| Delivery: collaborative classroom |
Data Integrity and Document Management
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 1 day | |
| Pricing from £450 per attendee | |
| Delivery: collaborative classroom |
EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |
GCP and Clinical Research Update - Hot Inspection Topics
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 1 day | |
| Pricing from £450 per attendee | |
| Delivery: collaborative classroom |
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3
In-house & bespoke training
Optimising oversight for inspection compliance.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |
Medical Device Studies: Clinical Evidence
In-house & bespoke training
Gathering and using clinical evidence for CE marking and post-market compliance in line with the new MDR.
Rated by attendees to the public programme
Typically presented by Janette Benaddi (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
In-house & bespoke training
An essential overview of medical device clinical evaluations, clinical investigations, post-market clinical follow-up requirements and adverse event and vigilance reporting.
Rated by attendees to the public programme
Typically presented by Janette Benaddi (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |
Metrics and Earned Value in Clinical Research Projects
In-house & bespoke training
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.
Typically presented by Roger Joby (bio)
| Typical duration: 3 days | |
| Delivery: collaborative classroom |
Practical Implementation of a Human Factors Study
In-house & bespoke training
This training focuses on the practical and logistical aspects of planning, preparing and performing human factors studies for medical devices and combination products.
Typically presented by Richard Featherstone (bio)
| Delivery: collaborative classroom |
Practical Implementation of GCP in Veterinary Field Studies
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Rachel Anderson (bio) , Donna Taylor (bio) , Jenny Webster (bio)
| Typical duration: 2 days | |
| Pricing from £800 per attendee | |
| Delivery: collaborative classroom |