Use of the Data by the Recipient Sample Clauses

Use of the Data by the Recipient. The Recipient agrees: (i) to use the Data for the sole purpose of conducting Research that is directed and overseen by the Recipient Researcher; and (ii) to use the Data in compliance with all applicable federal, state, local, international, health authority and institutional laws, rules, regulations, orders and guidelines (including the Data Protection Legislation); and (iii) to maintain, store and treat the Data in the same manner, and with the same level of care (but in no event less than a reasonable level of care), as the Recipient would maintain, store and treat its own proprietary or confidential information to prevent its unauthorized transfer, disclosure or publication, as applicable; and (iv) not to use the Data to attempt to determine, or determine, the identity of any of the research participants participating in the Enroll-HD Study whose (A) genotypic or phenotypic data is included in the Data and/or (B) data and/or biological materials were used to derive data included in the Data; and (v) if the Recipient is established in a country outside of the European Economic Area (and, as of, or at any time after, the effective date of this Agreement, either (A) that country does not hold a European Commission decision finding that such country provides an adequate level of protection or (B) the Recipient does not hold a European Commission decision finding that it provides an adequate level of protection), to (1) agree with CHDI in its capacity as the "data exporter" (as defined in the Standard Contractual Clauses) of the Data and (2) comply with each of the contractual clauses set out in the Standard Contractual Clauses in its capacity as the "data importer" (as defined in the Standard Contractual Clauses) of the Data (to the extent that the Standard Contractual Clauses are superseded or replaced by equivalent standard data protection clauses adopted by the European Commission in accordance with the examination procedure referred to in Article 93(2) of the GDPR (the "Updated Contractual Clauses"), the Recipient acknowledges and agrees that, as of the date the Updated Contractual Clauses become effective, the Standard Contractual Clauses shall cease to apply to any and all transfers of personal data and the Updated Contractual Clauses shall supersede and replace the Standard Contractual Clauses from such effective date; provided, that, Annex B to the Standard Contractual Clauses shall be deemed to be incorporated into, and form part of, the Updated C...

Use of the Data by the Recipient. The Recipient agrees: (i) to use the Data for the sole purpose of conducting Research that is directed and overseen by the Recipient Researcher; and (ii) to use Data in compliance with all applicable federal, state, local, international, health authority and institutional laws, rules, regulations, orders and guidelines; and (iii) to maintain, store and treat the Data in the same manner, and with the same level of care (but in no event less than a reasonable level of care), as the Recipient would maintain, store and treat its own proprietary or confidential information to prevent its unauthorized transfer, disclosure or publication, as applicable; (iv) not to use Data to attempt to determine, or determine, the identity of any of the Enroll-HD Study research participants from which the Data were collected; and (v) subject to, and except as expressly permitted by, this Agreement or otherwise expressly consented to in writing by CHDI, not to transfer or disclose the Data to any third party; and (vi) subject to, and except as expressly permitted by, this Agreement or otherwise expressly consented to in writing by CHDI, not to publish the Data; and (vii) to, upon the written request of CHDI, immediately and appropriately destroy or discard the Data of any Enroll-HD Study research participant from which the applicable Data were collected who has requested that their Data no longer be stored and used for Research.

Use of the Data by the Recipient. The Recipient agrees: (i) to use the Data for the sole purpose of conducting HD-Related Research that is directed and overseen by the Recipient Researcher; and (ii) to use the Data in compliance with all applicable federal, state, local, international, health authority and institutional laws, rules, regulations, orders and guidelines; and (iii) to maintain, store and treat the Data in the same manner, and with the same level of care (but in no event less than a reasonable level of care), as the Recipient would maintain, store and treat its own proprietary or confidential information to prevent its unauthorized transfer, disclosure or publication, as applicable; and (iv) to the extent the Data includes data collected from research participants in clinical studies, not to use the Data to attempt to determine, or determine, the identity of any of the research participants from which the Data were collected; and (v) subject to, and except as expressly permitted by, this Agreement or otherwise expressly consented to in writing by CHDI, not to transfer or disclose the Data to any third party; and (vi) subject to, and except as expressly permitted by, this Agreement or otherwise expressly consented to in writing by CHDI, not to publish the Data; and (vii) to report to CHDI any use, transfer, disclosure or publication of the Data not expressly permitted by this Agreement within 10 days of becoming aware of any such use, transfer, disclosure or publication.