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

9-10 May 2024 - Online webinar
Also on: 5 Aug 2024

Cover all the aspects of clinical evaluation in line with the European medical device regulations and applicable guidance documents

Presented by Janette Benaddi (bio)

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Clinical Quality Management Systems Training Course

Clinical Quality Management Systems

23-24 May 2024 - Online webinar
Also on: 19 Sep 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

10 Jun 2024 - Online webinar
Also on: 4 Oct 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 Jun 2024 - Online webinar
Also on: 23 Oct 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

2-3 May 2024 - Online webinar
Also on: 16 Sep 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 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

18 Sep 2024 - Online webinar

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

22 Jul 2024 - Online webinar
Also on: 6 Dec 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

20-21 May 2024 - Online webinar
Also on: 25 Jul 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

1 Jul 2024 - Online webinar
Also on: 22 Nov 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 Service Providers including CRO (Contract Research Organisation) and CMOs oversight to comply with ICH GCP (Good Clinical Practice) R3 Training Course

Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3

18-19 Apr 2024 - Online webinar
Also on: 24 Jun 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

10-11 Jul 2024 - Online webinar
Also on: 11 Nov 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

21-22 May 2024 - Online webinar
Also on: 16 Sep 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

11 Jul 2024 - Online webinar
Also on: 25 Nov 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

15-16 Jul 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 Rachel Anderson (bio)
Donna Taylor (bio)
Jenny Webster (bio)

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Very kind and attentive

Nicolas Oviedo, Medical Affairs Specialist, Baxter Healthcare Corp

I enjoyed the structure and the way the webinar is organized with a very knowledgeable and interesting speaker.

Emina Omeragic, Director Clinical Regulatory Affairs, TRiCares GmbH

I am brand new to the CER world and was hoping to better understand the layout. Janette did a fantastic job helping me to accomplish this. She made it very easy to get a clear picture of the expectations of completing a CER.

Tena Green, Medical Writer/Clinical Consultant, SunMed LLC

It was very organized and beautifully presented

Tena Green, Medical Writer/Clinical Consultant, SunMed, LLC

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

The training was clear and comprehensive.

Alexandre Jauniaux, Head of division, Federal Agency for Medicines and Health Products

My goal was to gain an overview on the regulations on medical devices and the general procedure of clinical evaluations. This goal has been achieved.

Hoda Bazafkan, Clinical Evaluations Manager, Geräte GmbH

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