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Electronic Informed Consent ... bringing the clinical trial home
GDPR and Clinical Trials: Compliance and Harmonization
Staying Safe on the Way to Innovative Therapeutic Options - Phase I Trials in Research Clinics
EMA Clinical Trials Information System (CTIS)
Towards the Implementation of Personalised Medicine
Electronic Informed Consent ... bringing the clinical trial home
Computerized System Validation in Clinical Research
COVID-19 in the Paediatric Population
Electronic Informed Consent… a global perspective
How to navigate your clinical trials in times of Corona
Traceability in Clinical Trials: Challenges of the new EU TMF/eTMF Guideline
The Patient Centricity Effect – How it benefits Patients, Sites and Sponsors – Practical cases from paediatric studies
GDPR CoC – EUCROF members
GDPR CoC – BVMA
Training: Essentials of Paediatric Clinical Research
Validation of Computerized Systems in GCP Environment
GDPR and CTR Interplay. One Year Later. Understandings and Questionings.
Risk-based and Remote Monitoring
Understanding the Crisis around the P-Values: Statistical Methods for the 21st Century
“Doing More with Data: Data Anonymization and Pseudonymization under the GDPR”
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