Updated course – stay compliant with ICH GCP E6 (R3)!
Stay compliant with data protection laws and ensure ethical conduct in clinical trials with this professionally developed, interactive GDPR in Clinical Research online training course. Updated to reflect the latest regulatory expectations, this course explores the critical implications of the General Data Protection Regulation (GDPR) – effective since May 2018 – on the conduct and management of clinical trials.
Designed for professionals across all areas of clinical research, this course is also valuable for patients and participants seeking to understand how their personal data is protected during clinical trial participation.
In an increasingly regulated research environment, GDPR compliance is vital. This course helps ensure that your organisation’s internal policies and clinical trial practices are fully aligned with data protection legislation, helping you avoid costly penalties and regulatory setbacks that could impact trial timelines and data integrity.
Who Should Take This Course?
This training is suitable for:
- Clinical Research Professionals (CRAs, CTAs, Coordinators)
- Investigators and Site Staff
- Regulatory Affairs and Ethics Specialists
- Data Managers and IT/Privacy Officers
- Clinical Trial Participants and Patient Advocates
- Whether you’re managing data collection, informed consent, or handling participant records, this course provides a clear understanding of your responsibilities under GDPR.
Download Course Summary Leaflet
Click the link above to explore the complete course content in our PDF leaflet.
