Sponsor Confidential Information has the meaning set forth in Section 5.06(a).
Sponsor Confidential Information means any information relating to (1) the proprietary, nonpublic inputs to the Base Case Projections, (2) the Project Documents, (3) the Construction Plans, and (4) the Financial Statements of the Sponsor Parties.
Sponsor Confidential Information shall have the meaning set forth in Section 11(a).
Examples of Sponsor Confidential Information in a sentence
In connection with requests made pursuant to clauses (iii) or (iv) of this Section 4.3(a) (a “Disclosure Order”), each Party shall use Commercially Reasonable Efforts to notify the other Party prior to disclosing any non-public term or condition of any of the Participation Agreement, Transaction Documents or any Sponsor Confidential Information and use Commercially Reasonable Efforts to prevent or limit such disclosure.
Sponsor understands and agrees that nothing in this Agreement interferes with UMD’s right to conduct research similar or related to the subject of the Research Project (“Related Research”), provided that such Related Research is conducted separately from the Research Project and does not involve the unauthorized use of Sponsor Confidential Information.
Sexual harassment by officials.No official holding any elected office of the city shall engage in, encourage, or permit – by action or inaction – behavior constituting sexual harassment of any other City official or employee.
As used herein, the Sponsor Confidential Information shall also include the Deliverables, Sponsor Inventions, and any other data, methods, results, conclusions, information and/or other deliverables made, conceived, reduced to practice or otherwise generated in connection with this Agreement, whether by Sponsor or PPD.
Institution and/or Investigator will notify Sponsor immediately of any loss, compromise, or unauthorized use or disclosure of any part or all of Sponsor Confidential Information.
More Definitions of Sponsor Confidential Information
Sponsor Confidential Information is defined as information and material that is regarded by SPONSOR as confidential and proprietary to SPONSOR and received from SPONSOR, and which is designated as confidential or which by its nature may reasonably be considered to be confidential. WSU shall limit access the SPONSOR Confidential Information to those of its employees with a need to have access to such SPONSOR Confidential Information. WSU shall not disclose SPONSOR Confidential Information to any third party and shall use SPONSOR Confidential Information solely for the purpose of conducting the Program. WSU's obligations under this Section 8 shall be limited to a period of five (5) years from receipt of SPONSOR Confidential Information. WSU shall not have any obligation of confidentiality with respect to any SPONSOR Confidential Information that:
Sponsor Confidential Information shall not include information or materials that: (i) were in the possession of the CDAC before receipt from the Sponsor; (ii) were or become available to the public through no fault of the CDAC; (iii) have been received in good faith by the CDAC from a third party who does not owe a duty of confidentiality to the Sponsor; (iv) have been independently developed by the CDAC without any use of Sponsor Confidential Information; or (v) are required to be disclosed by law.
Sponsor Confidential Information means (a) any and all scientific, technical, business, regulatory, or financial information in whatever form (written, oral, electronic or visual) that is delivered or otherwise disclosed to HJF, CRO, RedHill, Sites, Site Principal Investigators, or Principal Investigator (“Recipient”), by or on behalf of HJF or RedHill or its designees (“Discloser”) for the purpose of conducting the Study, including the Protocol, the financial terms of this Agreement; (b) all approvals and correspondence with or from an IRB or other entities with oversight responsibilities for the Study, including ethics committees or data safety monitoring committees, all Study correspondence, all Study Drug accountability forms, and all CRFs (collectively, the “Study Documentation”); (c) all Study Data and (d) information that a reasonable person familiar with the Study would consider to be confidential or proprietary from the context or circumstances of disclosure; provided, however, that (i) Study Drug Sponsor and HJF are co-exclusive owners of all Study Data pursuant to Section 9.2 (Study Data and Materials) and are free to use their own Confidential Information subject to Section 7 (Publication); (ii) Protocol Principal Investigator may use and/or publish Study Data solely in accordance with this Agreement; (iii) Sites and Site Principal Investigators may use and/or publish Study Data solely in accordance with the applicable Site contract, substantially similar to those terms and conditions applicable to the Parties under this Agreement; (iv) the U.S. Government may use and/or publish Study Data and Technical Data in accordance with the OTA; and (v) a Discloser is free to use its own Sponsor Confidential Information for which it is the Discloser.
Sponsor Confidential Information includes, without limitation, any and all of the clinical data and research results, technical and non-technical data,
Sponsor Confidential Information includes without limitation: (i) Sponsor’s or its Affiliate’s business records, oral or electronic communications, financial information, business practices, trade secrets, know-how, intellectual property, materials, inventions, formulas, compounds, devices, specifications, designs, plans, methods, software, data, technical information, concepts, procedures, processes, business plans, current and past distribution and production arrangements (oral or written), facilities, employees, marketing and sales strategies, business opportunities and strategic plans; (ii) information related to or arising from any proprietary compounds of Sponsor or Sponsor’s Affiliates that is developed by Medpace in connection with the performance of the Services hereunder; (iii) Sponsor Arising IP; (iv) information that is generated or developed by or received from Study Sites by Medpace in connection the performance of Medpace’s Services under the applicable Task Order; and (v) the terms of this Agreement.
Sponsor Confidential Information means all information (and all tangible and intangible embodiments thereof) that is disclosed by or on behalf of the Sponsor to the the Institution, including, without limitation, any scientific, technical, trade or business information possessed or obtained by, developed for or given to Sponsor which is treated by Sponsor as confidential or proprietary. “Sponsor Confidential Information” includes, without limitation, the Protocol, completed CRFs, signed Informed Consent Forms, Study Device, accountability forms, IRB approvals and correspondence, Study correspondence and the Results; see, however, sections 5.4 and 6, below, for Institution’s rights to use and publish Results. „Důvěrné informace zadavatele“ znamenají veškeré informace (a veškeré jejich hmotné a nehmotné provedení), které zadavatel sdělí nebo jsou sděleny jeho jménem zdravotnickému zařízení, , mimo jiné včetně vědeckých, technických, obchodních nebo firemních informací, které zadavatel vlastní, získal, vyvinul nebo mu byly předány a s nimiž zadavatel nakládá jako s důvěrnými nebo soukromými. „Důvěrné informace zadavatele“ zahrnují mimo jiné protokol, vyplněné formuláře CRF, podepsané formuláře informovaného souhlasu, hodnocený zdravotnický prostředek, formuláře dopočitatelnosti zařízení, souhlasy IRB a korespondenci, korespondenci ke studii a výsledky; pokud však jde o práva zdravotnického zařízení používat a publikovat výsledky, podívejte se na oddíly 5.4 a 6 níže.
Sponsor Confidential Information means all information (and all tangible and intangible embodiments thereof) that is disclosed by or on behalf of the Sponsor to the Institution or the Investigator, whether or not labeled “confidential”, including, without limitation, any scientific, technical, trade or business information possessed or obtained by, developed for or given to Sponsor which is treated by Sponsor as confidential or proprietary. “Sponsor Confidential Information” includes, without limitation, the Protocol, completed CRFs, signed Informed Consent Forms, Study Device, accountability forms, IRB approvals and correspondence, Study correspondence and the Results; see, however, sections studie mohly být zařazeny. Formuláře pro sběr dat subjektů hodnocení budou předány zadavateli xxxx xxx pověřeným osobám ve formě nebo na elektronickém médiu dle pokynů zadavatele xxxx xxx pověřených osob. Na žádost zadavatele xxxx xxx pověřených osob opraví zdravotnické zařízení nebo zkoušející neprodleně veškeré chyby a/nebo opomenutí ve formulářích pro sběr dat subjektů hodnocení týkajících se studie a zpřístupní zadavateli a/xxxx xxx pověřeným osobám opravené formuláře a podpůrné záznamy k další kontrole. Zkoušející souhlasí s xxx, že podepíše prohlášení uvedené v záznamech studie každého subjektu hodnocení nebo ve formuláři pro sběr dat subjektů hodnocení, které potvrzuje, že provedl kontrolu formuláře pro sběr dat subjektů hodnocení a ověřil, že informace v něm obsažené jsou přesné a obsahují léčbu, péči a příhody, které proběhly v rámci účasti daného subjektu hodnocení ve studii.