Regulatory Request definition

Regulatory Request has the meaning set forth in Section 11.2(b) (Limits on Use and Disclosure).
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Regulatory Request means any valid subpoena, order or written request from a Governmental Authority having jurisdiction over a Party or its Affiliates or third-party service provider for Confidential Information or Program Information.
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Regulatory Request means a communication in relation to the Agreement Personal Data, from any relevant competent regulator or similar body, or supervisory authority;
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Examples of Regulatory Request in a sentence

  • A timeframe for reviewing the Regulatory Request and preparing the Compliance Review Plan will be agreed between the parties, taking into account the requirements of applicable Data Protection Laws and the urgency of the matter as well as doing everything commercially reasonable given the circumstances and nature of the Services and Products to meet specific time frames set by the relevant Supervisory Authority in connection with the Regulatory Request.

  • If NeoSystems, any of its Sub-processors, or Client believe that it is not possible to meet a specific time frame set by the relevant Supervisory Authority in connection with the Regulatory Request, NeoSystems and/or its Sub-processor will provide reasonable assistance to Client to explain this to the relevant Supervisory Authority.

  • A timeframe for reviewing the Regulatory Request and preparing the Compliance Review Plan will be agreed between the parties, taking into account the requirements of Applicable Data Protection Laws and the urgency of the matter as well as doing everything commercially reasonable given the circumstances and nature of the Services to meet specific time frames set by the relevant authority in connection with the Regulatory Request.

  • Before taking any such step pursuant to a Regulatory Request, NGX shall act in accordance with any reasonable instruction given by Astellas in relation to such Regulatory Request unless action is required to be taken urgently by the relevant governmental or regulatory authority, in which case NGX shall inform Astellas of such action as soon as possible thereafter.

  • If ATIV, any of its Sub-processors, or Organizer believe that it is not possible to meet a specific time frame set by the relevant authority in connection with the Regulatory Request, ATIV and/or its Sub-processor will assist Organizer to explain this to the relevant authority, including by providing details of the reasons why the timeframes cannot be met.

  • Before taking any such step pursuant to a Regulatory Request, ASTELLAS shall act in accordance with any reasonable instruction given by BASILEA in relation to such Regulatory Request unless action is required to be taken urgently by the relevant Regulatory Authority, in which case ASTELLAS shall inform BASILEA of such action as soon as possible thereafter.

  • Before taking any such step pursuant to a Regulatory Request, NGX shall act in accordance with any reasonable instruction given by CHRP in relation to such Regulatory Request unless action is required to be taken urgently by the relevant governmental or regulatory authority, in which case NGX shall inform CHRP of such action as soon as possible thereafter.

  • If Cvent, any of its Sub-processors, or the Customer believe that it is not possible to meet a specific time frame set by the relevant authority in connection with the Regulatory Request, Cvent and/or its Sub-processor will assist Customer to explain this to the relevant authority, including by providing details of the reasons why the timeframes cannot be met.

  • Tr. (Sonoiki) 331-32.291 Tr. (Beckham) 369-72.Regulation Department inquiries in 2008, and 892 in 2009.292 She also testified that there were days when the firm received between 40 and 70 requests.293Enforcement estimates there were far fewer requests, based on its evaluation of Beckham’s logs for 2008 and 2009, and the Management Committee Regulatory Request Charts provided by Wedbush, purportedly listing requests from March to July, 2008.

  • A timeframe for reviewing the Regulatory Request and preparing the Compliance Review Plan will be agreed between the parties, taking into account the requirements of European Data Protection Laws and the urgency of the matter as well as doing everything commercially reasonable given the circumstances and nature of the Services to meet specific time frames set by the relevant authority in connection with the Regulatory Request.


More Definitions of Regulatory Request

Regulatory Request has the meaning set forth in Section 19(b).
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Regulatory Request has the meaning given to that term in clause 0; Related Body Corporate: a body corporate which is deemed by Applicable Law to be related, including by way of control or by having the same holding company; Representatives: Global Prime ’s representatives as set out in item Error! Reference source not found. of the Schedule, and includes such other person or persons nominated by Global Prime from time to time; Schedule: the Schedule of this Agreement (as amended from time to time);
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Regulatory Request shall have the meaning set forth in Section 4.8(c)(iii).
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Regulatory Request means any written request by an applicable Regulatory Authority or other Governmental Authority to amend, cancel, withdraw, or surrender any Marketing Authorization, or to take any step in relation thereto. 1.70 “Safety Related Information” means all adverse events, special situations (such as medication errors or medication management), other documentation such as source data and decisions related to individual case reports, minutes from safety meetings, signal detection 8 ACTIVE/99458941.1
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Related to Regulatory Request

  • Regulatory Requirement means any law, regulation or court order, or any rule, direction, guideline, code, notice or restriction (whether or not having the force of law) issued by any regulatory authority, governmental agency (including tax authority), clearing or settlement bank or exchange, or industry or self-regulatory body, whether in or outside Hong Kong, to which HKICL, we or any other Participant or the respective affiliates or group companies, or you are subject or are expected to comply with from time to time.

  • Regulatory Requirements means all applicable federal and state statutes, regulations, regulatory guidance, judicial or administrative rulings, requirements of Governmental Contracts and standards and requirements of any accrediting or certifying organization, including, but not limited to, the requirements set forth in a Product Attachment.

  • Requesting Authority means the Authority making a request under this MoU.

  • Regulatory Filing means any filing with any Governmental Authority with respect to the research, development, manufacture, distribution, pricing, reimbursement, marketing or sale of a Product.

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval (but excluding Pricing Approval) in any particular jurisdiction other than the U.S.

  • Regulatory Approval Application means any application submitted to an appropriate Regulatory Authority seeking any Regulatory Approval.

  • Regulatory Rules means all corporate and securities laws, regulations, rules, policies, notices, instruments and other orders of any kind whatsoever which may, from time to time, apply to the implementation, operation or amendment of this Plan or the Options granted from time to time hereunder including, without limitation, those of the applicable Regulatory Authorities.

  • Regulatory Order means an order issued by a permitting authority that requires compliance with:

  • Controlling Authority means the Minister administering the Tasmanian State Service Act 1984.

  • Regulatory Authority means any federal, national, multinational, state, county, city, provincial, or local regulatory agency, department, bureau or other governmental entity with authority over the marketing, commercialization, manufacture or sale of a pharmaceutical product in the Territory, including the FDA in the United States and the EMA in the EU.

  • Regulatory Authorities means the Commissions and the Exchange;

  • Regulatory Body means those government departments and regulatory, statutory and other entities, committees, ombudsmen and bodies which, whether under statute, rules, regulations, codes of practice or otherwise, are entitled to regulate or investigate the matters dealt with in this Agreement or any other affairs of the Provider or the Department, including, without limitation Ofsted, the European Commission and the European Court of Auditors;

  • FDA means the United States Food and Drug Administration and any successor agency thereto.

  • Marketing Authorization means all approvals, licenses, registrations or authorizations of any federal, state or local regulatory agency, department, bureau or other governmental entity, necessary for the manufacturing, use, storage, import, transport, marketing and sale of Licensed Products in a country or regulatory jurisdiction.

  • Approval Application means a BLA, NDA or similar application or submission for a Product filed with a Regulatory Authority in a country or group of countries to obtain marketing approval for a biological or pharmaceutical product in that country or group of countries.

  • Participating Certified Clinical Nurse Specialist means a Certified Clinical Nurse Specialist who has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Securities Regulatory Authorities means the securities commission or similar regulatory authority in each province and territory of Canada that is responsible for administering the Canadian securities legislation in force in such jurisdictions;

  • Regulatory Floodway means the channel of a river or other watercourse and the adjacent land areas that must be reserved in order to discharge the base flood without cumulatively increasing the water surface elevation more than a designated height.

  • Canadian Securities Regulatory Authorities means the securities regulatory authorities in each of the provinces and territories of Canada;

  • Regulatory Approval means any and all approvals (including MAA Approval, and Pricing and Reimbursement Approval, if applicable), licenses, registrations, permits, notifications and authorizations (or waivers) of any Regulatory Authority that are necessary for the manufacture, use, storage, import, transport, promotion, marketing, distribution, offer for sale, sale or other commercialization of a Product in any country or jurisdiction.

  • Marketing Approval Application or “MAA” means a New Drug Application (or its equivalent), as defined in the U.S. Food, Drug and Cosmetic Act and the regulations promulgated thereunder, or any corresponding or similar application, registration or certification in any country.

  • Regulatory entity means any board, commission, agency,

  • Regulatory Services Provider means the organization which provides regulatory services to BSEF pursuant to a Regulatory Services Agreement.

  • securities regulatory authority or “SRA” means a body created by statute in any Canadian or foreign jurisdiction to administer securities law, regulation and policy (e.g. securities commission), but does not include an exchange or other self regulatory entity;

  • Applicable Insurance Regulatory Authority means, when used with respect to any Insurance Subsidiary, the insurance department or similar administrative authority or agency located in (x) the state or other jurisdiction in which such Insurance Subsidiary is domiciled or (y) to the extent asserting regulatory jurisdiction over such Insurance Subsidiary, the insurance department, authority or agency in each state or other jurisdiction in which such Insurance Subsidiary is licensed, and shall include any Federal insurance regulatory department, authority or agency that may be created in the future and that asserts regulatory jurisdiction over such Insurance Subsidiary.

  • Drug Approval Application means an application for Regulatory Approval required before commercial sale of a Product as a pharmaceutical product in a regulatory jurisdiction.