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"Update
on New European Data Protection Rules for US Companies providing
Clinical Trials, Cross Border Research and Healthcare Services"
Get a comprehensive update on the current
GDPR and European Data Protection regulations applying to the US
healthcare industry. Learn how the new transatlantic relationship
between the new Trump administration and the European Union is
changing significantly the rules of the game.
You may choose to register at any of the
two following dates:
Thursday April 24, 2025, 13:30 to 15:30 ET, 10:30 to 12:30 pm Pacific Time
Tuesday April 29, 2025, 13:30 to 15:30 ET, 10:30 to 12:30 pm Pacific Time
Main goals:
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Understand the latest
European privacy updates (e.g., GDPR, EDPB guidance,
Data Privacy Framework) impacting cross-border research,
clinical trials and healthcare services in general.
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Navigate
how U.S. privacy policy
shifts under the Trump administration may affect data
transfers, compliance posture, and risk exposure.
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Identify
how EU patient rights,
consent, and data handling obligations apply to
U.S.-led research, clinical trials and digital health activities.
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Gain
practical tools to ensure ongoing
GDPR compliance and
ethical data practices in clinical and healthcare
activities.
Contents:
Module 1: What’s New in
European Privacy Law (30 minutes)
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Recent
GDPR updates relevant to healthcare services, clinical research and patient data
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EU
Court rulings (e.g., Schrems II impacts) and DPA enforcement
trends
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The
EU-U.S. Data Privacy Framework: current status, limitations, and
outlook
Module 2: U.S. Privacy
Policy Shift Under Trump (30 minutes)
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Expected changes to federal privacy enforcement (FTC, OCR, HHS)
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Potential weakening of international data transfer commitments
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Challenges balancing HIPAA and GDPR in research and healthcare
systems
Module 3: Data Compliance
in EU-US Research & Clinical Trials (40 minutes)
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Applying GDPR to U.S.-sponsored clinical trials (data subject
rights, retention, consent)
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Best
practices for data mapping, cross-border contracts, and
anonymization
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Tools:
Standard Contractual Clauses (SCCs), Data Transfer Impact
Assessments (DTIAs), and ethics board alignment
Live Q&A & Strategic
Takeaways (20 minutes)
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Participant Q&A with instructor
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Downloadable “2025 GDPR Checklist for Research & Healthcare”
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Bonus:
Crosswalk of EU-U.S. Data Privacy Duties for Clinical Teams
Instructor:
Aldo F. Mosti
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Global
privacy and data protection expert with 15+ years in
European data protection regulations
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EMEA
Director and Partner of the EuroPrivacy Institute
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Expert in
GDPR applied to
cross-border research and clinical trials
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Speaker
at varios events and international venues
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Advisor
to university IRBs and European research consortia
Cost:
The registration fee for this online live course is
$79.00 per participant and includes: 1)
Certificate-Diploma with high
curricular value issued by the Europrivacy Institute 2) Teaching material
in PDF;
3) Downloadable compliance toolkit; 4) EU-U.S. Data Transfer
Contract Templates (sample clauses).
*You will receive the Zoom link in
24 hours after your registration and payment is verified. No need to
install anything. Fast speed internet required.
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