Study Staff. Sponsor and Sponsor designees shall process Study Staff personal data to the extent needed for the Study and research purposes. Such personal data shall at all times be processed in accordance with Data Protection Laws. Sponsor (or Sponsor’s designee) shall deliver privacy notices to the Principal Investigator and Study Staff regarding the processing of their personal data by Sponsor. Institution and Principal Investigator each agrees to provide reasonable assistance to Sponsor (or Sponsor’s designee) in issuing, distributing and collecting such consents and/or transparency/privacy notices as applicable.
Study Staff. Institution shall be responsible for distributing a GDPR transparency notice to, and if required by Sponsor, for obtaining consent of, each Study Staff in order for Sponsor and its designees to process Study Staff personal data to the extent needed for the Study purposes. Such personal data shall at all times be processed in accordance with Data Protection Laws. Sponsor (or Sponsor’s designee) shall provide the transparency notice and any required consent to Institution in a form approved by Sponsor for distribution. If consent is required by Sponsor, Sponsor will have discretion whether to accept the Study Staff signature on the Delegation of Responsibilities Log, provided by Sponsor prior to initiation, will be evidence of acceptance this provision.
Study Staff. Institution, through Principal Investigator, shall supervise Study Staff in their performance of the Study and ensure that all Study Staff are qualified to perform the duties assigned to such person. Institution shall take reasonable steps to inform Study Staff of their obligations under this Agreement.
Study Staff. Institution shall be responsible for distributing a GDPR transparency notice to, and if required by Sponsor, for obtaining consent of, each Study Staff in order for Sponsor and its designees to process Study Staff personal 6.25. Personál studie: Zdravotnické zařízení zodpovídá za předání oznámení o transparentnosti podle GDPR každému členovi Personálu studie, a pokud si to Zadavatel vyžádá, za získání souhlasu data to the extent needed for the Study purposes. Such personal data shall at all times be processed in accordance with Data Protection Laws. Sponsor (or Sponsor’s designee) shall provide the transparency notice and any required consent to Institution in a form approved by Sponsor for distribution. If consent is required by Sponsor, Sponsor will have discretion whether to accept the Study Staff signature on the Delegation of Responsibilities Log, provided by Sponsor prior to initiation, will be evidence of acceptance this provision. každého člena Personálu studie, aby mohl Zadavatel a jím pověřené osoby zpracovávat osobní údaje Personálu studie v rozsahu potřebném pro účely Studie. Tyto osobní údaje budou za všech okolností zpracovávány v souladu s Právními předpisy o ochraně osobních údajů. Zadavatel (nebo jím pověřená osoba) poskytne Zdravotnickému zařízení oznámení o transparentnosti a případný požadovaný souhlas ve formě schválené Zadavatelem k předávání. Pokud bude Zadavatel požadovat souhlas, bude na jeho rozhodnutí, zda přijme podpis Personálu studie v záznamu o delegování povinností, který Zadavatel dodá před zahájením, jako důkaz přijetí tohoto ustanovení.
7.1 Principal Investigator and Study Staff (“Permitted Attendees”) may be invited to attend and participate in meetings regarding the Study, including, but not limited to, investigator, study coordinator and/or results meetings (“Study Meetings”). To the extent that Permitted Attendees attend a Study Meeting, the parties agree that there will be no additional compensation for attendance or participation at such Study Meeting. If the Principal Investigator or Study Staff is retained by Sponsor to perform services at the Study Meeting, the terms and obligations of such services will be subject to a separate agreement. Permitted Attendees may be provided with hotel accommodations, meals and transportation to and from the Study Meeting (collectively, “Accommodation”). The value of such Accommodation may be disclosed pursuant to applicable Sponsor’s state and federal legal reporting requirement...
Study Staff. Sponsor and its designees shall process Study Staff personal data to the extent needed (i) to conduct the Study; (ii) to satisfy requirements under Applicable Laws, including review by regulatory authorities; and (iii) storage in databases for use in selecting investigators and institutions for future clinical trials. Such personal data shall at all times be processed in accordance with Data Protection Laws. Institution and Principal Investigator each agrees to provide reasonable assistance to Sponsor (or Sponsor’s designee) in issuing, distributing, and collecting such consents and/or transparency/privacy notices as applicable, to or from Principal Investigator and other Study Staff.
Study Staff. Institution, through Principal Investigator, shall be responsible for distributing a GDPR transparency notice to, and if required by Sponsor, for obtaining consent of, each Study Staff in order for Sponsor and its designees to process Study Staff personal data to the extent needed for the Study purposes. Such personal data shall at all times be processed in accordance with Data Protection Laws. Sponsor (or Sponsor’s designee) shall provide the transparency notice and any required consent to Institution in a form approved by Sponsor for distribution. If consent is required by Sponsor, Sponsor will have discretion whether to accept the Study Staff signature on the Delegation of Responsibilities Log, provided by Sponsor prior 6.20. Personál studie: Zdravotnické zařízení prostřednictvím Hlavního zkoušejícího zodpovídá za předání oznámení o transparentnosti podle GDPR každému členovi Personálu studie, a pokud si to Zadavatel vyžádá, za získání souhlasu každého člena Personálu studie, aby mohl Zadavatel a jím pověřené osoby zpracovávat osobní údaje Personálu studie v rozsahu potřebném pro účely Studie. Tyto osobní údaje budou za všech okolností zpracovávány v souladu s Právními předpisy o ochraně osobních údajů. Zadavatel (nebo jím pověřená osoba) poskytne Poskytovateli zdravotních služeb oznámení o transparentnosti a případný požadovaný souhlas ve formě schválené Zadavatelem k předávání. Pokud bude Zadavatel požadovat souhlas, bude na jeho rozhodnutí, zda to initiation, will be evidence of acceptance this provision. přijme podpis Personálu studie v záznamu o delegování povinností, který Zadavatel dodá před zahájením, jako důkaz přijetí tohoto ustanovení.
Study Staff. All personnel performing services on the Study under the direct supervision and instruction of Institution and Investigator, including, but not limited to the Investigator, sub-investigators, study coordinators, study nurses, employees, agents and/or subcontractors of Institution.
Study Staff. Sponsor and its designees shall process Study Staff personal data to the extent needed (i) to conduct the Study; (ii) to satisfy requirements under Applicable Laws, including review by regulatory authorities; and (iii) storage in databases for use in selecting investigators and institutions for future clinical trials. Such personal data shall at all times be processed in accordance with Data Protection Laws. Institution and Principal Investigator each agrees to provide reasonable assistance to Sponsor (or Sponsor’s designee) in issuing, distributing, and collecting such consents and/or transparency/privacy notices as applicable, to or 6.21. Personál studie: Zadavatel a jím pověřené osoby zpracovávají osobní údaje Personálu studie v rozsahu potřebném (i) pro provádění Studie; (ii) pro splnění požadavků platných Právních předpisů, včetně kontroly ze strany regulačních orgánů; a
Study Staff. Site will ensure that all Study Staff have the medical, technical and/or laboratory expertise to conduct the Study and are available to support and carry out Site’s obligations under this Agreement. Further, Institution will ensure that before commencing any work on the Study, all Study Staff are subject to written obligations to Institution under which they (i) are bound to obligations of confidentiality and non-use with respect to Confidential Information (as defined below) that are consistent with the terms of this Agreement; and (ii) assign and otherwise effectively vest in Institution any and all rights that such Study Staff might otherwise have in the results of their work without any obligation of Sponsor to pay any royalties or other consideration to such Study Staff.
Study Staff. Sponsor and its designees shall process Study Staff personal data to the extent needed (i) to conduct the Study; (ii) to satisfy requirements under Applicable Laws, including review by regulatory authorities; and (iii) storage in databases for use in selecting investigators and institutions for future clinical trials..
