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What you need to know about data privacy in clinical trials
The General Data Protection Regulation (GDPR) is a significant advancement of consumer data protection rights. The European member states agreed to a set of principles that would penalize organizations that don’t safeguard personal identifying information (PII). While it was hailed as the most consumer-friendly data protection regulation at the time of passing, many countries followed the EU’s lead and harmonized their laws to match – with some even surpassing- GDPR’s principles-based approach to data privacy.
If your team or clinical trial operates in the EU, California, S Korea, Australia, or a dozen other countries, your data could be subject to strict privacy laws. Violating GDPR, PIPA, APP, or CCPA, among others, have serious consequences for your program. Learn how to mitigate risk and keep on the right side of regulators.
Topics include:
- Global clinical trial hotspots and their data privacy laws
- How to comply with data regulations and mitigate the risk of a breach
- Roles in GDPR-harmonized data privacy regulations
- How to operationalize best practices in your organization