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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”