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Virtual Event

2025年6月25日 (水) 午後 1:00 - 2025年6月25日 (水) 午後 5:00

(Central Europe Standard Time)

4051 Basel, Switzerland

Mastering GDPR Compliance in Clinical Trials

This virtual live training course covers the essential concepts of EU and UK data protection laws that sponsors need to consider when running clinical trials.

Early-Bird rate for DIA Industry Members Available!

DAYS

HOURS

MINUTES

SECONDS

概要

This virtual live training course covers the essential concepts of EU and UK data protection laws that sponsors need to consider when running clinical trials.

Understanding and complying with data protection laws, such as the General Data Protection Regulation (GDPR), is crucial for clinical trial sponsors to ensure legal compliance, protect participant rights, maintain data security, and uphold ethical standards in clinical research. It is also often a prerequisite for obtaining regulatory approval to conduct the clinical trial.

This training course will equip participants with the knowledge and tools to navigate GDPR requirements confidently and ensure clinical trials meet the (sometimes) onerous GDPR requirements. Case studies will be used throughout to provide context.

Participants benefit from the hands-on experience of instructors who are experts in this area.

特集トピック

    • GDPR Overview
    • Lawful Processing of Study Subject Data
    • Transparency
    • Role of the Site
    • Engaging vendors
    • Cross-Border Transfers
    • Investigators and Study Personnel
    • Safety Data Reporting Activities
    • Data Treatment Principles and Accountability
    • Security and Personal Data Breaches

参加対象

  • This course is designed for professionals involved in Clinical Trials such as:

    • Commercial and Non-commercial sponsors of clinical trials
    • CROs
    • Consultants

学習目的

  • This virtual live training course is designed for professionals working in:

    • Pharmacovigilance (including EU QPPVs)
    • Drug Safety and Risk Management
    • Signal Management and Safety Science
    • Pharmacoepidemiology
    • Information Technology
    • Pharmacovigilance Consultancies and Service Providers
    • Quality and Compliance

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