Studijní centrum. Neither Party shall transfer (or permit their processors to transfer) any Sponsor-Controlled Personal Data outside the European Equivalent Protection Area without ensuring that explicit consent of the Study Subject or another legal basis or derogation for the transfer exists under EU or EU Member State law. For purposes of this Agreement, “EU Equivalent Protection Area” means the area that comprises: (a) countries within the European Union, Iceland, Liechtenstein and Norway; and (b) countries, sectors in countries and international organizations that the European Commission may, from time to time, officially recognize as ensuring an adequate level of protection as provided for in Article 45 of the GDPR.
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Studijní centrum. Neither Party shall transfer (or permit their processors to transfer) any Sponsor-Controlled Personal Data outside the European Equivalent Protection Area without ensuring that explicit consent of adequate safeguards are in place (e.g. Standard Contractual Clauses recognized by the Study Subject or EU Commission) unless another legal basis or derogation for the transfer exists under EU or EU Member State law. For purposes of this Agreement, “EU Equivalent Protection Area” means the area that comprises: (a) countries within the European Union, Iceland, Liechtenstein and Norway; and (b) countries, sectors in countries and international organizations that the European Commission may, from time to time, officially recognize as ensuring an adequate level of protection as provided for in Article 45 of the GDPR.
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Samples: Clinical Trial Agreement
Studijní centrum. xxxxxxxxxxx
6.5. Neither Party shall transfer (or permit their processors to transfer) any Sponsor-Controlled Personal Data outside the European Equivalent Protection Area without ensuring that explicit consent of the Study Subject or another legal basis or derogation for the transfer exists under EU or EU Member State law. For purposes of this Agreement, “EU Equivalent Protection Area” means the area that comprises: (a) countries within the European Union, Iceland, Liechtenstein and Norway; and (b) countries, sectors in countries and international organizations that the European Commission may, from time to time, officially recognize as ensuring an adequate level of protection as provided for in Article 45 of the GDPR. Institution transfers personal data exclusively within the EU, as defined above.
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Samples: Clinical Trial Agreement