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

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

More @ IPI Academy

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

More @ IPI Academy

Clinical Research - A Different Approach to Successful Project Delivery

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

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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

More @ IPI Academy

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

More @ IPI Academy

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

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Cognitive Testing in Clinical Drug Trials: Successful Test Selection and Integration

In-house & bespoke training

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.

Typically presented by John E. Harrison (bio)

Delivery: collaborative classroom

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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

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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

More @ IPI Academy

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

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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

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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

More @ IPI Academy

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

More @ IPI Academy

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

More @ IPI Academy

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

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Very knowledgeable and presented information in a concise, easy to understand way

Joanna Faraj, Quality System Manager, Mitsubishi Tanabe Pharma Europe

Very knowledgeable and presented information in a concise, easy to understand way

Joanna Faraj, Quality System Manager, Mitsubishi Tanabe Pharma Europe

I'm very delighted with the course, the presentation and the speakers.

Cuong Nguyen, Associate Specialist, Clinical Research, MSD Animal Health Innovation GmbH

I thought it was overall a very good course that I would recommend people to take.

Marte Sønnervik, Clinical Study Coordinator, PHARMAQ

Laura Brown's webinar gave me more confident in data integrity she presented all the necessary information to gain my confident. I really appreciate it.

Kheira Heddi, Quality Assurance Officer, SGSUK

It was good to actively take part as this makes you think harder about what you have been told.

Vicki Paterson, Senior Research Associate, Frontier Science Scotland

I really enjoyed the course and Rachel, Jenny and Donna were wonderfully engaging presenter and given us lots of opportunity to ask the questions. The course was mix of theory & few practical exercises. I took away lots of things which I can easily apply at my work .

Kritika Sengar Chauhan, Associate Specialist, Clinical Research, MSD Animal Health Innovation GmbH

The speaker demonstrated a deep knowledge of all themes presented during the course. Sessions were well organized and enough time was dedicated to each of them.

Vincenzo Velleca, Global Safety Operations, Zambon SpA

The content was very useful for my daily work. The presentation was well prepared and the speaker made it easy to listen online.

Christiane Rederath, Clinical Research Associate, MSD Animal Health Innovation GmbH


The presenters were incredibly knowledgeable in their subject areas and was able to convey complex information, in an easily digestible way. Overall, a very good summary of Clinical evidence for medical devices.

Hannah Vince-Drew, Clinical Research Supervisor, Bedfont Scientific