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30 March 2022 - EU Clinical Trial Regulation 536/2014 (CTR): Transitional Provisions and New Concepts

Personalised Medicine Current Applications in Clinical Research and Regulatory Framework

Trial Master File Archiving and the Decommissioning of Computerised Systems Used in Clinical Trials

Future of Clinical Trials: Navigating Complexities to Increase Investigator Satisfaction

The Home Care Services - Useful Tool for Decentralized Clinical Trials

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