Data transfer is a crucial issue for companies that work in the life sciences sector and is a highly regulated and ever-changing regime. Typical personal data categories transferred from organisations to third parties include clinical trial data, data relating to unlicensed/compassionate use, health technology assessment data, transfers of value records for transparency reports, patient information enquiries for marketed products, and other patient and employee personal data.
Join us for a one-hour webinar to review the recent changes and learn how to navigate this evolving regulatory framework. |
| Topics will include: |
- The Safe Harbor certification programme
and
life after Schrems
- An overview of the new EU General
Data Protection
Regulation regime
- Key issues facing the industry in the EU
and
United States
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