Management Forum courses now available at IPI Academy - visit IPI for an updated experience and a broader selection of courses and subjects

In-house & bespoke training:
Clinical

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.


 

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

View details

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

View details

Clinical Trial Monitoring

In-house & bespoke training

This course will assure monitors understand the importance of compliance with GCP standards, and how these apply to monitoring clinical trials including during the pandemic and in the future.

Typically presented by Laura Brown (bio)

Delivery: collaborative classroom

View details

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 key difference it compares with the Clinical Directive 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

View details

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

View details

EU Clinical Trial Regulation 536/2014: Overview and Implementation

In-house & bespoke training

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

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

View details

GCP and Clinical Research Update - Hot Inspection Topics

In-house & bespoke training

This course provides recent updates on the EU Clinical Trial Regulation, other EU, MHRA and FDA requirements, consideration for managing Covid-19 for studies in the future and 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

View details

Managing Vendor/CRO/CMO Oversight

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

View details

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

View details

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

View details

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 Tamsin Dawson (bio) , Donna Taylor (bio) , Jenny Webster (bio)

Typical duration: 2 days
Pricing from £800 per attendee
Delivery: collaborative classroom

View details

Overall, I would recommend the webinar to people who are starting a career in clinical trials as it gives a good overview of all aspects of GCP.

Laure Bidois, Senior Advisor Regulatory Affairs, knoell

Very good presentation and useful information with links, examples and clips which made it more interesting.

Kianoosh Khaksar, Compliance Specialist, Lundbeck

Excellent course, excellent trainer. Found it very valuable and will be taking away knowledge gained to further improve processes and understanding within my department.

Sarah Collins, Pharmacovigilance Manager, PharSafer

Fantastic speaker. I truly enjoyed listening to Janette, her ability to relate real life examples helped make sense of the topics.

Melissa Patterson, Associate Manager, Corporate Clinical Compliance, Edwards Lifesciences

Very on target; Management Forum does an excellent job.

Chiara Delia, Global Regulatory Affairs Specialist, Chiesi Farmaceutici S.p.a.

It was a well done webinar, the speakers were very competent and experienced. The content was informative

Helena Metzker, Clinical Research Associate, MSD Animal Health Innovation

Understanding RFP and RFI were achieved, KPI session was very helpful and I learnt about oversight plan which I never knew about... Laura was very good, provided great content of the subject matter and discussions included were good and relevant.

Stephanie Yearwood, Senior Vendor Management Coordinator , IQVIA

Very nice webinar which gave a good overview of the CTR and the CTIS portal. I liked the parts where the part 1 and part 2 was presented as I think this is not straightforward to understand. Also, I like the small quizzes that were done.

Ellen Due Horup, Compliance Manager, ALK-Abelló

Laura was very helpful and went out of her way to make sure we understood everything. This course was regarding EU and FDA only but when asked about UK she made sure she got up some extra information regarding this and was very helpful.

Bethany Roome, Clinical Operations Manager, Torbay Pharmaceuticals

Very thorough and covered a lot of topics

Christine Woodward, Pharmacovigilance Manager, Drug Safety Solutions Limited