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

Clinical Evaluation of Medical Devices: The Clinical Evaluation Report Training Course

Clinical Evaluation of Medical Devices: The Clinical Evaluation Report

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

Presented by Adrian Keene (bio)
Séverine Oudin (bio)

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Clinical Quality Management Systems Training Course

Clinical Quality Management Systems

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)

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Clinical Research - A Different Approach to Successful Project Delivery Training Course

Clinical Research - A Different Approach to Successful Project Delivery

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)

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Clinical Research Project Management Training Course

Clinical Research Project Management

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)

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Clinical Trial Monitoring Training Course

Clinical Trial Monitoring

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)

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Clinical Trial Regulatory Requirements Training Course

Clinical Trial Regulatory Requirements

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)

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

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

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)

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Data Integrity and Document Management Training Course

Data Integrity and Document Management

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)

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EU (European Union) Clinical Trial Regulation 536/2014: Overview and Implementation Experience Training Course

EU Clinical Trial Regulation 536/2014: Overview and Implementation Experience

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)

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GCP (Good Clinical Practice) and Clinical Research Update - Hot Inspection Topics Training Course

GCP and Clinical Research Update - Hot Inspection Topics

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)

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Managing Vendor/CRO (Contract Research Organisation)/CMO (Contract Manufacturing Organisation) Oversight Training Course

Managing Vendor/CRO/CMO Oversight

15-16 Jan 2024 - Online webinar
Also on: 18 Apr 2024

Optimising oversight for inspection compliance

Presented by Laura Brown (bio)

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Medical Device Studies: Clinical Evidence Training Course

Medical Device Studies: Clinical Evidence

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)

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Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course

Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

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)

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Metrics and Earned Value in Clinical Research Projects Training Course

Metrics and Earned Value in Clinical Research Projects

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)

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Practical Implementation of GCP (Good Clinical Practice) in Veterinary Field Studies Training Course

Practical Implementation of GCP in Veterinary Field Studies

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.

Presented by Donna Taylor (bio)
Jenny Webster (bio)

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In-house training

We can provide any of our courses on an in-house basis - at your location or online, with a programme and presenters tailored to your exact requirements. If you require training for multiple staff members, contact us to see how we can work with you.

Previous attendees said...

“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

“Excellent and again would only receive this expected type of learning and understanding with the course by IPI Academy. I know that I will have a comprehensive understanding to use the information learned and apply at my job with IPI Academy webinars. I do not get that elsewhere.”

Angela Turner, RA Director,

“Very well done and would recommend to others”

Jaclyn Verrow, Director, TMF Compliance & Oversight, Vertex Pharmaceuticals

“Overall, the webinar was fantastic. Thank you for such solid course.”

Remy Serge Manzi-Muhire, Senior Clinical Product Risk Specialist, BOSTON SCIENTIFIC CORPORATION

“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

“very interesting
a lot of information and sometimes very fast - so very good to have the material available”

Virginie Graide, QMS Lead, argenx

“Mary-Ann is super nice and professional. She gave a clear presentation and respond to our questions quickly and professionally. ”

Xue Li, Clinical Regulation Affairs, Geuder AG