Our latest COVID-19 information/status - including self-paced online learning from our training partner Falconbury

Training & Courses:

Management Forum’s clinical training courses cover all aspects of clinical research. Our expert speakers will cover the latest regulatory updates and key topics relevant for all clinical trial professionals.


Our spring/summer 2020 programme of London-based courses has been cancelled due to the COVID-19 outbreak. We are taking bookings for our Autumn events, but we are also working to deliver courses and content online. Please contact us if you are interested in an on-site or online version of any of our courses, tailored to your company's needs.

A two-day course that will ensure you comply with new regulatory requirements.

Clinical Quality Management Systems

19-20 Nov 2020

Also on: 17 May 2021

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 existing Directive requirements.

Clinical Trial Regulatory Requirements

28-29 Jan 2021

Also on: 5 Jul 2021

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.

Data Integrity and Document Management

5 Oct 2020

Also on: 5 Mar 2021

This course will provide an essential understanding to help with compliance with the new regulation and associated implementing acts and other texts for carrying out clinical trials in the EU

EU Clinical Trial Regulation: Overview and Implementation

19-20 Oct 2020

Also on: 22 Apr 2021

This course provides an update on recent changes to ICH GCP R2, EU Clinical Trial Regulation and guidance and will discuss how these changes have been implemented

This one-hour webinar will help you understand what the impact of GDPR has been on drug development
25 February 2019 – 2pm (GMT)

We can customise this course to meet your requirements.

Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R&D projects you need to outsource

Managing Vendor/CRO/CMO Oversight

8-9 Oct 2020

Also on: 26 Apr 2021

This must-attend new event will provide an essential overview of the opportunities and challenges presented by orphan drug regulation.

Regulatory Strategies for Orphan Drugs

23 Sep 2020

Also on: 10 Mar 2021

Ensure your clinical trials comply with the latest focus on GCP inspections and develop your own quality risk management principles and procedures

Risk Management for Clinical Research

28 Sep 2020

Also on: 22 Mar 2021

The small group allowed for good interaction between participants.

Jacques Wodelet , Quality Manager , JWC

The course was well done and the speaker was well prepared and enthusiastic.

Valentina Cenacchi, Senior PK scientist, Chiesi Farmaceutici SpA

Professional, engaging, informative, useful.

James O'Donoghue, Director Medical Writing, PRA Health Sciences

It was very good course. There are too many good points to list! The course was very relevant to my job and will help me in most aspects of my work. Laura was very clear and knowledgeable. She empowers participants for discussion and welcomed feedback from all participants.

Kaushik Patel, Category Manager, BTG PLC

Very good and worthwhile attending.

Christopher Rollinson, Research Governance Manager, University Hospitals Plymouth NHS Trust

Very interesting training, excellent for a clear and well structured introduction to Risk Management in Clinical Research.

Myriam Mouhib, Clinical Assessment Manager, JT International

Laura was passionate, knowledgable and entertaining. I particularly liked the group work sessions, which gave us time to digest and use the information just obtained.

Josy Giordano, Regulatory Affairs Manager, Nestec SA

I really enjoyed the course. Content was very interesting, presentation material well done and it was possible to ask lots of questions. Laura is a very experienced speaker and she knows how to get the audience's attention.

Yvonne Wiggenhauser, Process Document Manager , Takeda Pharmaceuticals International AG

The speaker was very friendly and engaging and I liked the interactive nature of the course.

Richard O'Callaghan, Quality Officer, Teva Pharmaceuticals Ireland

I think this course has been very good.

Sidse Schjøtz, Compliance Manager, ALK