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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)
| Typical duration: 1 day | |
| Pricing from £500 per attendee | |
| Delivery: collaborative classroom |
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects
In-house & bespoke training
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.
Typically presented by Zuzanna Kwade (bio)
| Typical duration: 1 day | |
| Pricing from £500 per attendee | |
| Delivery: collaborative classroom |
Clinical Evaluation of Medical Device Software and Software as a Medical Device
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.
Rated by attendees to the public programme
Typically presented by Zuzanna Kwade (bio)
| Typical duration: 1 day | |
| Pricing from £500 per attendee | |
| 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 Steve Curran (bio) , Joanne E Stewart (James) (bio)
| Typical duration: 2 days | |
| Pricing from £1,000 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 £1,000 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
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 3 days | |
| Pricing from £1,260 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)
| Typical duration: 2 days | |
| Pricing from £1,000 per attendee | |
| 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 £1,000 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)
| Typical duration: 90-minutes days | |
| Pricing from £200 per attendee | |
| 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 £500 per attendee | |
| Delivery: collaborative classroom |
Digital Technology and Personalisation in Patient Support Programmes
In-house & bespoke training
Learn how to build digital technology that is specifically aligned to match with the patient, the clinical study, the disease and the treatment programme.
Typically presented by Graham Howieson (bio)
| Typical duration: 1 day | |
| Pricing from £500 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 £1,000 per attendee | |
| Delivery: collaborative classroom |
GCP and Clinical Research Update - Hot Inspection Topics
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 1 day | |
| Pricing from £500 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 £1,000 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 Joanne E Stewart (James) (bio)
| Typical duration: 2 days | |
| Pricing from £1,000 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
| Typical duration: 2 days | |
| Pricing from £1,000 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: Half-day days | |
| Pricing from £350 per attendee | |
| Delivery: collaborative classroom |
Microbiomics in Clinical Trials
In-house & bespoke training
Explore the microbiome and its high clinical relevance, as well as learning about the different methodology used in microbiomic clinical trials.
Typically presented by Nikolaj Sørensen (bio)
| Typical duration: Half-day days | |
| Pricing from £350 per attendee | |
| Delivery: collaborative classroom |
Navigating ICH GCP E6 (R3): What You Need to Know
In-house & bespoke training
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.
Typically presented by Laura Brown (bio)
| Pricing from £500 per attendee | |
| 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 £1,000 per attendee | |
| Delivery: collaborative classroom |
Real World Evidence (RWE), Real World Data (RWD) and the Application of Artificial Intelligence (AI) in Pharma
In-house & bespoke training
A deep dive into the importance of real world evidence (RWE), real world data (RWD) and artificial intelligence (AI) in pharmaceuticals.
Typically presented by Graham Howieson (bio)
| Typical duration: 1 day | |
| Pricing from £500 per attendee | |
| Delivery: collaborative classroom |
Risk Management for Clinical Research
In-house & bespoke training
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.
Rated by attendees to the public programme
Typically presented by Laura Brown (bio)
| Typical duration: 1 day | |
| Pricing from £500 per attendee | |
| Delivery: collaborative classroom |
Software Automation in Research and Development (R&D) Clinical Trials
In-house & bespoke training
This course will help delegates gain a better understanding of the software automation technology driving change within the clinical trials landscape.
Typically presented by Graham Howieson (bio)
| Typical duration: 1 day | |
| Pricing from £500 per attendee | |
| Delivery: collaborative classroom |
Utilising Patient Adherence Data and Digital Tools to Improve Patient Outcomes
In-house & bespoke training
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.
Typically presented by Graham Howieson (bio)
| Typical duration: 1 day | |
| Pricing from £500 per attendee | |
| Delivery: collaborative classroom |