All Courses
Here is a list of all our courses available for you to take.
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Good Clinical Practice E6 R3
Introducing our newly updated, interactive, and engaging online GCP training course, now aligned with the latest ICH GCP E6 Revision 3 guidance.
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Good Documentation Practice (GDocP)
This professionally developed Good Documentation Practice (GDocP) course explores data integrity and document requirements in detail.
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Informed Consent
NOW HALF PRICE!
This course provides the user with a firm understanding of the background and practical implications of the valid Informed Consent process.
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Pharmacovigilance: Drug Safety and Regulations
This course provides the user with a firm understanding of pharmacovigilance and its relationship with drug safety.
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Clinical Project Management Training
This course will explain in everything you need to know about becoming an effective project manager within this field, from study start up right through to closeout.
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Good Clinical Practice (E6 R2)
Incorporates the ICH GCP E6 R2 guidance, and the new E6 R3 draft update due to be released in late 2023
CPD Points Available: 6
Available in other languages.
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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.
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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.
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Good Laboratory Practice
GLP regulates the practices of scientists working on the safety testing of prospective drugs.
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Medical Devices
Incorporating the new MDR and ISO 14155:2020 to develop knowledge and understanding of the Medical Devices.
CPD Points Available: 6
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Good Clinical Practice (E6 R2) – German
This is the new updated course of GCP for 2022 translated into German.
Verfügbare CPD-Punkte: 6
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Good Clinical Practice (E6 R2) – Spanish
This is the new updated course of GCP for 2022 translated into Spanish.
Puntos CPD disponibles: 6
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Good Clinical Practice (E6 R2) – French
This is the new updated course of GCP for 2022 translated into French.
Points de DPC Disponibles: 6
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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.
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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.
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Good Manufacturing Practice (GMP)
Good Manufacturing Practice (GMP) describes the minimum standard that a medicines manufacturer must meet in their production processes.
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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.
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Medical Devices – Quality Management Systems
ISO 13485:2016 was written to support Medical Device manufacturers in designing Quality Management Systems (QMS)...
Save Money
Sign up for our GxP group courses and save £97
You will gain access to:
Good Clinical Practice (E6 R3)
Good Clinical Laboratory Practice (GCLP)
Good Manufacturing Practice (GMP)
Good Documentation Practice (GDocP)
Guaranteed Success
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.
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Device Compatibility
All of our online courses are accessible on desktop, tablet and mobile.
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Instant Certification
Once completed , you will get a digital certificate which you can print.
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Fun & Engaging
Fun, engaging and can be taken on any device, anywhere, anytime.