All Courses
Here is a list of all our courses available for you to take.
GxP
Good Clinical Practice (E6 R2)
Good Clinical Laboratory Practice (GCLP)
Good Manufacturing Practice (GMP)
Good Documentation Practice (GDocP) & Essential Documents.
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You will gain access to:
Good Clinical Practice (E6 R2)
Good Clinical Laboratory Practice (GCLP)
Good Manufacturing Practice (GMP)
Good Documentation Practice (GDocP) & Essential Documents
Good Clinical Practice (E6 R2)
This is the new updated course of GCP for 2022.
CPD Points Available: 6
Available in other languages.
GCP Refresher
This is a professionally developed training course which incorporates the ICH E6 R2 update implemented in June 2017, along with the new EU Clinical Trials Regulation which became live on the 31st January 2022.
Clinical Trials Audit Preparation
The course describes what investigational medicinal product sponsors, contract research organisations and clinical investigators can expect when they undergo inspection or audit.
Good Laboratory Practice
GLP regulates the practices of scientists working on the safety testing of prospective drugs.
Good Documentation Practice (GDocP) & Essential Documents
This is a professionally developed, interactive and engaging online course essential for anyone working in Clinical Research.
Medical Devices
Incorporating the new MDR and ISO 14155:2020 to develop knowledge and understanding of the Medical Devices.
CPD Points Available: 6
Good Clinical Practice (E6 R2) – German
This is the new updated course of GCP for 2022 translated into German.
Verfügbare CPD-Punkte: 6
Good Clinical Practice (E6 R2) – Spanish
This is the new updated course of GCP for 2022 translated into Spanish.
Puntos CPD disponibles: 6
Good Clinical Practice (E6 R2) – French
This is the new updated course of GCP for 2022 translated into French.
Points de DPC Disponibles: 6
Clinical Research Associate (CRA) Training
This course goes through the whole clinical trial process and also includes aspects of Good Clinical Practice and Good Documentation Practice/Essential Documents.
Essential Documents
This is a professionally developed, interactive and engaging online course that will provide an overview of essential documents, including which stage of the Clinical Trial process they will normally be generated.
Good Manufacturing Practice (GMP)
Good Manufacturing Practice (GMP) describes the minimum standard that a medicines manufacturer must meet in their production processes.
GDPR for Clinical Trials and Patients
Examines the implications of the recent General Data Protection Regulation (GDPR) that became effective on the 25th May 2018 on those working within Clinical Research.
Medical Devices – Quality Management Systems
ISO 13485:2016 was written to support Medical Device manufacturers in designing Quality Management Systems (QMS)...
Good Clinical Laboratory Practice
GCLP guidance identifies the systems required and procedures to be followed within an organisation.
Managing Clinical Trials During COVID-19
A short course to help with managing clinical trials during Covid-19.
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Unique, Exciting &
Interactive E-Learning Courses.
Learning has never been easier than with Training Online 4U. Our extensive range of online courses covers all your personal and professional development needs.
Device Compatibility
All of our online courses are accessible on desktop, tablet and mobile.
Instant Certification
Once completed , you will get a digital certificate which you can print.
Fun & Engaging
Fun, engaging and can be taken on any device, anywhere, anytime.