Regulatory Requests. PFPC will provide information and documentation relating to the Fund or other assistance relating to such information and documentation as the Fund may reasonably request to help the Fund respond to any government or regulatory request, including but not limited to a subpoena or request for information, provided, however, that if responding to such a request would cause an undue burden on PFPC or would cause PFPC to bear undue expense, PFPC at its option may decline such request or shall be entitled to such fees or reimbursement of expenses as agreed to by the Fund and PFPC.
Regulatory Requests. If a Receiving Party receives a Regulatory Request to disclose any Confidential Information of the Disclosing Party, the Receiving Party shall, to the extent permitted by Applicable Law:
Regulatory Requests. At Customer’s request, CribMaster will assist Customer in the event of an investigation by a competent regulator, including a data protection regulator or similar authority, if and to the extent that such investigation relates to the Processing of Personal Information by CribMaster on behalf of Customer in accordance with these Terms and Conditions. CribMaster reserves the right to charge a reasonable fee to Customer for such requested assistance, to the extent permitted by applicable law.
Regulatory Requests. Cost associated with implementing technology and/or services requested by MHCC in support of privacy and security may be dispersed at CRISP’s discretion across users that are assessed a fee to access or receive electronic health information.
Regulatory Requests. Within [**] Business Days after receipt, NewCo shall provide ADCT any formal or informal requests received from any Regulatory Authority in the Territory related to the Products. NewCo shall manage preparation of a response to such requests; provided that, at NewCo’s reasonable request and cost and expense, ADCT or its designee shall provide assistance in preparing a response that addresses matters raised by the Regulatory Authority in such request, according to a timeline reasonably agreed by the Parties. NewCo shall submit all responses before the due date set by the Regulatory Authority and NewCo shall provide ADCT a copy of the final response for its approval as soon as reasonably practicable (but not less than [**] Business Days prior to such submission due date) and ADCT will conduct such review on a timely basis; provided, however, NewCo may submit its response without regard to ADCT's review if comments arising from such review are not received by NewCo at least [**] Business Days prior to the applicable due date. Certain confidential information contained in this document, marked by [**], has been omitted because ADC Therapeutics SA has determined that the information (i) is not material and (ii) would likely cause competitive harm to ADC Therapeutics SA if publicly disclosed.
Regulatory Requests. In addition to the Regulatory Filings referenced in (i) and (ii) above, Cipla will also be responsible for any Regulatory Filings that may be required to comply with Applicable Law or requested by the applicable Regulatory Authority in relation to Promotional Materials and Adverse Drug Experiences after the Product is approved for a Pulmonary Indication in the applicable country in the Territory.
Regulatory Requests. After the completion of the Services, Biovest shall provide any information and assistance reasonably requested by AYTU, at AYTU’s expense, for any regulatory filing or regulatory compliance activities relating to the Services arising from a request for information from a regulatory agency.
Regulatory Requests. After the completion of the Research Project, Humabs agrees to provide any information and assistance reasonably requested by MedImmune for any regulatory filing or regulatory compliance activities relating to the Research Project arising from a request for information from a regulatory agency, and if such reasonable assistance exceeds [***], MedImmune shall reimburse Humabs at [***]. Humabs agrees that [***].
Regulatory Requests. FIS and Client are subject to continuing oversight and supervisory authority by various federal regulatory agencies (“Federal Regulators”). FIS and Client each acknowledge and agree that when requested by a Federal Regulator, the Agreement and any information related to the Agreement may be disclosed by either party to a Federal Regulator (as required by Federal Law) without prior notice to the other party and without disclosure to the other party of the Federal Regulator’s request.
Regulatory Requests. FIS and Client are subject to continuing oversight and supervisory authority by various federal regulatory agencies (“Federal Regulators”). FIS and Client each acknowledge and agree that EID: 2685 PLID: 248707 when requested by a Federal Regulator, the Agreement and any information related to the Agreement may be disclosed by either party to a Federal Regulator (as required by Federal Law) without prior notice to the other party and without disclosure to the other party of the Federal Regulator’s request. EID: 2685 PLID: 248707 CONFIDENTIAL TREATMENT HAS BEEN REQUESTED FRAUD DETECTION AND IDENTITY SERVICES ADDENDUM Attachment 1 – Service Categories and Permissible Uses Client hereby certifies that it shall use the FIS Data provided through the Service in accordance with the applicable terms and conditions of the Addendum and solely for the Permissible Use associated with the Service as set forth below: Fraud Detection and Identity Services: • Address Analysis(1) • ID Authentication(1) • ID Verification(1) Identity Services: • ID Authentication(1) • ID Verification(1) Driver’s License Services: • ID Verification(2) Watch List Services: • ID Verification • OFAC Watch • OFAC Auto Attendant • Enhanced PEP/Fraud List Package Red Flag Services: • Red Flag Checklist
