GDPR in Clinical Trials
Understand how GDPR applies to clinical trials with this focused online training course. Learn how to manage personal data lawfully, ensure compliance with EU data protection regulations, and protect participant privacy throughout the trial process. Ideal for clinical research and regulatory professionals.
Good Manufacturing Practice (GMP)
Covering core GMP topics including quality systems, documentation, hygiene, production, warehousing, and distribution, the course also explores the role of GMP in laboratories, engineering, and trial sites — providing a functional, cross-departmental perspective.
Good Laboratory Practice (GLP)
This professionally developed Good Laboratory Practice (GLP) training course provides a comprehensive understanding of the regulatory requirements and operational standards governing non-clinical laboratory studies.
ICH Good Clinical Practice (including E6 R3) for Investigators
Gain essential knowledge with our ICH Good Clinical Practice (GCP) E6 R3 online training for investigators. Fully updated for 2025, this certified course meets global regulatory standards and includes 2 CPD points.
CPD Points Available: 2
Good Laboratory Practice (GLP) Refresher
Update your knowledge with our Good Laboratory Practice (GLP) refresher course. Aligned with the latest OECD guidance, this course reinforces core GLP principles for regulatory compliance in non-clinical research.
ICH Good Clinical Practice (GCP) Refresher (Including E6 R3)
Refresh your existing knowledge of ICH Good Clinical Practice while incorporating the latest E6 Revision 3 guidance. Ideal for those with prior GCP training, this course supports practical application in your clinical research role.
CPD Points Available: 4
Good Clinical Practice E6 R3
Stay compliant with global clinical trial standards through our ICH Good Clinical Practice (GCP) E6 R3 training course. Fully updated for 2025, this interactive course is suitable for all clinical research professionals and includes CPD accreditation and globally recognised certification.
CPD Points Available: 6
Informed Consent
Gain a clear understanding of the informed consent process in clinical trials with this interactive course. Updated for ICH GCP E6 R3, this accredited training is suitable for all clinical research professionals.
PVG: Drug Safety and Regulations
This course offers a comprehensive introduction to pharmacovigilance, providing a clear understanding of its vital role in ensuring drug safety and regulatory compliance throughout the product lifecycle.
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.
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.
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 Documentation Practice (GDocP) & Data Integrity
Gain essential knowledge in data integrity and Good Documentation Practices (GDocP) with this professionally developed course. Aligned with ICH GCP E6 R3, MHRA, and FDA guidelines, this training covers ALCOA++ principles, data governance, and compliance essentials for clinical research professionals.
Medical Devices
Gain a clear understanding of the EU Medical Device Regulation (MDR), ISO 14155:2020, and key FDA and MHRA guidance with this comprehensive training. Ideal for professionals involved in medical device clinical investigations, this course covers regulatory compliance throughout the development lifecycle.
CPD Points Available: 6
Medical Devices – Quality Management Systems
Understand the key principles and practical applications of ISO 13485:2016 in this comprehensive online course on Quality Management Systems (QMS) for medical devices. Learn how to develop, implement, and maintain a compliant QMS that supports regulatory certification and product safety.
Good Clinical Laboratory Practice
Stay compliant with global standards in clinical research laboratories with this updated Good Clinical Laboratory Practice (GCLP) course. Covering GCLP principles, quality systems, and regulatory expectations, this interactive training is ideal for professionals involved in the analysis of clinical trial samples.