Scheduled In-house

Clinical Research Training Courses

IPI Academy’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. 

 

 

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  • Next: 5-6 Aug 2024 Live online
  • Also: 27-28 Nov 2024 Live online

Clinical Evaluation of Medical Devices: The Clinical Evaluation Report

Live online

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

  • 12 CPD hours Focused
  • Presented by Janette Benaddi
  • Next: 19-20 Sep 2024 Live online

Clinical Quality Management Systems

Live online

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

  • 12 CPD hours Focused
  • Presented by Dr Laura Brown
  • Next: 4 Oct 2024 Live online

Clinical Research - A Different Approach to Successful Project Delivery

New for 2024

Live online

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.

  • 6 CPD hours
  • Presented by Roger Joby
  • Next: 26-28 Jun 2024 Live online
  • Also: 23-25 Oct 2024 Live online

Clinical Research Project Management

Updated for 2024

Live online

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

  • 18 CPD hours Focused
  • Presented by Dr Laura Brown
  • Next: 29-30 Jul 2024 Live online
  • Also: 2-3 Dec 2024 Live online

Clinical Trial Monitoring

Live online

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.

  • 12 CPD hours
  • Presented by Dr Laura Brown
  • Next: 16-17 Sep 2024 Live online

Clinical Trial Regulatory Requirements

Live online

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.

  • 12 CPD hours Focused
  • Presented by Dr Laura Brown
  • Next: 18 Sep 2024 Live online

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

New for 2024

Live online

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 Professor John E. Harrison
  • Next: 22 Jul 2024 Live online
  • Also: 6 Dec 2024 Live online

Data Integrity and Document Management

Live online

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.

  • 6 CPD hours Focused
  • Presented by Dr Laura Brown
  • Next: 25-26 Jul 2024 Live online
  • Also: 11-12 Nov 2024 Live online

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

Live online

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.

  • 12 CPD hours Focused
  • Presented by Dr Laura Brown
  • Next: 1 Jul 2024 Live online
  • Also: 22 Nov 2024 Live online

GCP and Clinical Research Update - Hot Inspection Topics

Live online

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.

  • 6 CPD hours Focused
  • Presented by Dr Laura Brown
  • Next: 24-25 Jun 2024 Live online
  • Also: 17-18 Oct 2024 Live online

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

Live online

Optimising oversight for inspection compliance

  • 12 CPD hours Focused
  • Presented by Dr Laura Brown
  • Next: 10-11 Jul 2024 Live online
  • Also: 11-12 Nov 2024 Live online

Medical Device Studies: Clinical Evidence

Live online

Gathering and using clinical evidence for CE marking and post-market compliance in line with the new MDR

  • 12 CPD hours Focused
  • Presented by Janette Benaddi
  • Next: 16-19 Sep 2024 Live online

Medical Device Studies: Regulatory Requirements and Adverse Event Reporting

Live online

An essential overview of medical device clinical evaluations, clinical investigations, post-market clinical follow-up requirements and adverse event and vigilance reporting.

  • 12 CPD hours Focused
  • Presented by Janette Benaddi
  • Next: 11 Jul 2024 Live online
  • Also: 25 Nov 2024 Live online

Metrics and Earned Value in Clinical Research Projects

New for 2024

Live online

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.

  • 4 CPD hours Masterclass
  • Presented by Roger Joby
  • Next: 15-16 Jul 2024 Live online
  • Also: 26-27 Nov 2024 Classroom

Practical Implementation of GCP in Veterinary Field Studies

Classroom, Live online

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.

  • 12 CPD hours Focused
  • Presented by Donna Taylor
  • + 2 more