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

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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

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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 existing 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

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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: 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 acts and other 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

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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

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GDPR and Implications on Drug Development - Webinar

In-house & bespoke training

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

Typical duration: 1 day
Pricing from £450 per attendee
Delivery: collaborative classroom

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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

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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

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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

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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 Julian Braidwood (bio) , Marie-Pascale Tiberghien (bio)

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

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Risk Management for Clinical Research

In-house & bespoke training

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

Rated by attendees to the public programme

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

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Personally I found the training very helpful as I realised how the concept of Data Integrity reflects in my daily work. I understood the big impact of Data Integrity in the Clinical Research which is becoming more and more digital.

Chiara Delmaestro, , Chiesi Farmaceutici S.p.A.

[Laura] is a good presenter, she has world of knowledge. She was also able to get open discussion with the participant which made the course more interesting.

Angelo Jacala, Director, Clinical QA, MEI Pharma

Great speaker, flexible attitude, and inclusive.

Syeda Ameernaz, Clincal safety Physician, Novocure

Very well organized in terms of content, very well presented, replies for every single question is addressed by the wonderful speaker and I truly enjoyed it and learned so much. Thank you it was excellent!

Nurit Birenboim, Regulatory Affairs Associate, Ayala Pharmaceutical

Janette is very nice and friendly. She has a lot of relevant knowledge and experience about the clinical evaluation process and the report. I learned a lot form her!

Dror Sever, Senior Device Information Scientist, Novo Nordisk

I thought this was a terrific webinar, lead by an excellent topic expert, and I feel much more confident about participating and/or leading the CER update at my company.

Juliana Pugmire, Clinical Research Consultant, Current Health

I found the details provided in the webinar and the additional resources/notes were very comprehensive. I enjoyed that there were multiple speakers/subject matter experts for specific areas in GCP planning to allow for better understanding of the key stakeholders in the planning process. The speakers were very informative and topics discussed were very relevant. The transition between topics kept attendees engaged for the entire time.

Abigail Harwood, Advisor Brand Maximization, Elanco New Zealand

Very interactive and stimulating.

Margherita Lerro, Study Manager, Menarini Ricerche

It was overall a very good webinar that gave a nice overview of the Clinical Evaluation proces. A shame it had to be a webinar due to the Covid-19 situation, it would have worked better if we could all meet in person and also have small conversations in breaks and so on.

Christina Frary, research audiologist, Demant

I think overall the webinar very good, instructive and informative.

Ban Eshqi, Scientific Affairs Pharmacist, CHEMIDEX PHARMA LTD