Examples of Site Parties in a sentence
The Site Parties shall allow Sponsor and/or CRO representatives to be present during any such visit as permitted by Law.
The Site Parties each acknowledge that the Sponsor may present at symposia, national or regional professional meetings, and publish in journals, theses or dissertations, or otherwise of their own choosing, methods and results of the Clinical Trial and in particular, but without limiting the foregoing, post a summary of Clinical Trial results in on-line clinical trials register(s) before or after publication by any other method.
The Site Parties shall permit authorized representatives of the Ethics Committee and Competent Authorities to have access to, copy and verify information relating to the Clinical Trial, as required by and in accordance with applicable Law.
Site Parties agree to help Sponsor obtain any express consents, as may be necessary in accordance with applicable Data Protection Law from the Site Investigator, and to the extent applicable and necessary from other Research Staff involved in the Clinical Study as well, for any intended processing of his/her/their Personal Data by Sponsor.
Sponsor shall ensure that such other participating sites adhere to the same terms and conditions with regards to Joint IP as Site Parties.
The Site Parties will not, and will ensure that the Research Staff will not, use the name or logo of the Sponsor and/or CRO or of any of its employees, nor the name of the Clinical Trial, nor the name of the Investigational Product, in any publicity, advertising or news release without the prior written approval of the Sponsor and/or CRO, such approval not to be unreasonably withheld.
The Site Parties shall allow Sponsor’s representatives to be present during any such visit.
The Site Parties shall make and retain records regarding the Clinical Trial as required by the Protocol, applicable Law, and in accordance with the Institution’s standard archiving procedures.
In the event that the Sponsor and /or CRO reasonably believes there has been any research misconduct in relation to the Clinical Trial, Site Parties shall provide all reasonable assistance to any investigation into any alleged research misconduct undertaken by or on behalf of the Sponsor and/or CRO, the results of which the Party on whose behalf the investigation was undertaken shall, subject to any obligations of confidentiality, communicate to the Principal Investigator.
For purposes of this Agreement and subject to clause 10 (Publication and Authorship), the Clinical Study results generated by Site Parties as disclosed through the CRF shall be considered Confidential Information of Sponsor and this clause 7 shall not provide Site Parties the rights granted hereunder to the Disclosing Party, where it relates to such Clinical Study results owned by Sponsor.