Disclosure by Pfizer Sample Clauses

Disclosure by Pfizer. In the interest of transparency relating to its relationships with investigators and study sites or to ensure compliance with applicable local law, Pfizer may publicly disclose the support it provides under this Agreement. Such a disclosure by Pfizer may identify both the Institution and the Principal Investigator, but will clearly differentiate between payments or other transfers of value to institutions and those made to individuals.
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Disclosure by Pfizer. In the interest of transparency relating to its financial relationships with investigators and study sites or to ensure compliance with Applicable Law, industry codes and Pfizer policies, Pfizer may, and (in certain cases) is required to, report or otherwise disclose publicly payments or other transfer of value to certain health care providers, teaching hospitals and other health care organizations, including Funding provided under this Agreement. These laws and codes, and their implementing regulations, collectively are referred to as “Transparency Obligations.” Pfizer may disclose in any lawful manner the terms of this Agreement and any other information to the extent necessary for Pfizer to meet its Transparency Obligations. The terms of the Agreement shall be publicly disclosed on Pfizer’s webpage (xxx.xxxxxx.xx) when the Agreement is made and for a period of 2 years thereafter.
Disclosure by Pfizer. In the interest of transparency relating to its financial relationships with investigators and Study/Registry sites or to ensure compliance with Applicable Law, industry codes and Pfizer policies, Pfizer may, and (in certain cases) is required to, report or otherwise disclose publicly payments or other transfer of value to certain health care providers, teaching hospitals and other health care organizations, including Funding provided under this Agreement. These laws and codes, and their implementing regulations, collectively are referred to as “Transparency Obligations.” Pfizer may disclose in any lawful manner the terms of this Agreement poskytovaných státem. 3.5 Žádné platby účtované třetím osobám. Příjemce grantu zajistí, aby žádnému subjektu studie, pojišťovně, orgánu veřejné moci ani jinému plátci ze strany třetích osob nebyly účtovány žádné platby za jakékoli činnosti související se Studií/Registrem prováděné Příjemcem grantu za použití Financování. 3.6
Disclosure by Pfizer. In the interest of transparency relating to its relationships with 2.2
Disclosure by Pfizer. In the interest of transparency relating to its relationships with investigators and study sites or to 2.2 Zverejnenie informácií zo strany spoločnosti Pfizer. V záujme transparentnosti ohľadom jej vzťahu so ensure compliance with applicable local law, Pfizer may publicly disclose the support it provides under this Agreement. Such a disclosure by Pfizer may identify both the Institution and the Principal Investigator, but will clearly differentiate between payments or other transfers of value to institutions and those made to individuals. skúšajúcimi a pracoviskami klinického skúšania, alebo aby sa zabezpečilo dodržiavanie príslušných právnych predpisov môže spoločnosť Pfizer zverejniť podporu, ktorú poskytuje v rámci tejto zmluvy. Takéto zverejnenie informácií zo strany spoločnosti Pfizer môže identifikovať inštitúciu aj hlavného skúšajúceho, ale jasne rozlíši medzi platbami alebo inými prevodmi hodnôt inštitúcii a jednotlivcom.
Disclosure by Pfizer. In the interest of transparency relating to its relationships with investigators and study sites or to ensure compliance with applicable local law, Pfizer may publicly disclose the support it provides under this Agreement. Such a disclosure by Pfizer may identify both the Health Services Provider and the Principal Investigator, but will clearly differentiate between payments or other transfers of value to legal persons and those made to individuals. Z veřejnění informací společností Pfizer. V zájmu transparence svých finančních vztahů se zkoušejícími a studijními pracovišti, nebo z důvodu zajištění dodržování příslušných místních právních předpisů, může společnost Pfizer zveřejnit finanční odměnu, kterou podle této Smlouvy poskytuje. Takové zveřejnění společností Pfizer může identifikovat jak Poskytovatele zdravotních služeb, tak i Hlavního zkoušejícího, ale bude zřetelně rozlišovat mezi platbami a jinými převody hodnot, jež jsou poukázány právnickým osobám, a těmi, jež jsou poukázány jednotlivcům.
Disclosure by Pfizer. Subcontractor acknowledges that Pfizer is subject to laws related to the collection and reporting of any payments or transfers of value to certain healthcare professionals and teaching hospitals (hereinafter: the “Payments to Healthcare Professionals”), including those laws, industry codes and accompanying implementing regulations, including section 6002 of the Affordable Care Act and The European Federation of Pharmaceutical Industries and Associations (EFPIA) Code on Disclosure of Transfers of Value (hereinafter, collectively, the “Transparency Laws”). Pfizer may disclose in any lawful manner the terms of Master Agreement and SOW, the support that Pfizer is providing under it, and any other information to the extent necessary for Pfizer to meet its obligations under the Transparency Laws including certain identifying information of healthcare professionals including names, National Provider Identifier, licensure number(s), specialty, and addresses. Subcontractor will provide Penta and/or Pfizer with all information Pfizer needs to meet its obligations under any Transparency Laws including identifying healthcare professionals and teaching hospitals that receive a payment or transfer-of- value stemming from Pfizer’s support under the Master Agreement and SOW, as well as the amounts and dates of those payments or transfers-of-value. In accordance with EFPIA Disclosure Code and local country privacy and legal requirements, a signed consent document may be collected. Subcontractor will provide the information required under this paragraph by accurately completing a data report in a format reasonably determined by Pfizer.
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Disclosure by Pfizer. In the interest of transparency relating to its financial relationships with investigators and study sites or to ensure compliance with applicable local law, Pfizer may publicly disclose the support it provides under this Agreement. Institution agrees that Pfizer may disclose in any lawful manner the terms of this Agreement, the support or funding that Pfizer is providing under this Agreement, and any other related information, to the extent necessary for Pfizer to meet its obligations under those laws, regulations and industry codes that require Pfizer to report payments or other transfers of value to certain healthcare professionals and teaching hospitals (collectively, the “Transparency Laws”). Transparency Laws include, without limitation, section 6002 of the U.S. Affordable Care Act and the EFPIA Code on Disclosure of Transfers of Value.

Related to Disclosure by Pfizer

  • Disclosure to FERC its Staff, or a State. Notwithstanding anything in this Article 22 to the contrary, and pursuant to 18 C.F.R. section 1b.20, if FERC or its staff, during the course of an investigation or otherwise, requests information from one of the Parties that is otherwise required to be maintained in confidence pursuant to this Agreement or the NYISO OATT, the Party shall provide the requested information to FERC or its staff, within the time provided for in the request for information. In providing the information to FERC or its staff, the Party must, consistent with 18 C.F.R. section 388.112, request that the information be treated as confidential and non-public by FERC and its staff and that the information be withheld from public disclosure. Parties are prohibited from notifying the other Parties to this Agreement prior to the release of the Confidential Information to the Commission or its staff. The Party shall notify the other Parties to the Agreement when it is notified by FERC or its staff that a request to release Confidential Information has been received by FERC, at which time the Parties may respond before such information would be made public, pursuant to 18 C.F.R. section 388.112. Requests from a state regulatory body conducting a confidential investigation shall be treated in a similar manner if consistent with the applicable state rules and regulations. A Party shall not be liable for any losses, consequential or otherwise, resulting from that Party divulging Confidential Information pursuant to a FERC or state regulatory body request under this paragraph.

  • Updated Information Submission by Developer The updated information submission by the Developer, including manufacturer information, shall occur no later than one hundred eighty (180) Calendar Days prior to the Trial Operation. Developer shall submit a completed copy of the Large Generating Facility data requirements contained in Appendix 1 to the Large Facility Interconnection Procedures. It shall also include any additional information provided to Connecting Transmission Owner for the Interconnection Feasibility Study and Interconnection Facilities Study. Information in this submission shall be the most current Large Generating Facility design or expected performance data. Information submitted for stability models shall be compatible with NYISO standard models. If there is no compatible model, the Developer will work with a consultant mutually agreed to by the Parties to develop and supply a standard model and associated information. If the Developer’s data is different from what was originally provided to Connecting Transmission Owner and NYISO pursuant to an Interconnection Study Agreement among Connecting Transmission Owner, NYISO and Developer and this difference may be reasonably expected to affect the other Parties’ facilities or the New York State Transmission System, but does not require the submission of a new Interconnection Request, then NYISO will conduct appropriate studies to determine the impact on the New York State Transmission System based on the actual data submitted pursuant to this Article 24.3. Such studies will provide an estimate of any additional modifications to the New York State Transmission System, Connecting Transmission Owner’s Attachment Facilities, or System Upgrade Facilities or System Deliverability Upgrades based on the actual data and a good faith estimate of the costs thereof. The Developer shall not begin Trial Operation until such studies are completed. The Developer shall be responsible for the cost of any modifications required by the actual data, including the cost of any required studies.

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