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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”