Regulatory Fine definition

Regulatory Fine means an insurable fine or civil monetary penalty imposed by a governmental or regulatory authority for a Data Breach.
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Regulatory Fine means any and all fines, regulatory assessments, penalties, withholdings, interest, and other monetary remedies similar amounts imposed by any Governmental Authority.
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Examples of Regulatory Fine in a sentence

  • On 24/25 February 2015, the following amendments to the Guidelines for Criminal Proceedings and Proceedings to Impose a Regulatory Fine ( Richtlinien für das Strafverfahren und das Bußgeldverfahren, RiStBV), which entered into force on 1 August 2015, were adopted by the responsible sub-committee of the Conference of German Justice Ministers.

  • The Guidelines for Criminal Proceedings and Proceedings to Impose a Regulatory Fine (RiStBV) contain special provisions for the protection of minors.

  • No. 86 of the Guidelines for Criminal Proceedings and Proceedings to Impose a Regulatory Fine: General (1) As soon as the public prosecutor learns of a criminal offence that can be prosecuted by means of private prosecution, he examines whether there is a public interest in an ex officio prosecution.

  • No. 207 of the Guidelines for Criminal Proceedings and Proceedings to Impose a Regulatory Fine: Informing the Federal Criminal Police Office (1) The Federal Criminal Police Office, Thaerstrasse 11, 65193 Wiesbaden is to be informed of the initiation of proceedings due to an offence relating to membership in or support of a proscribed organisation (sections 84, 85, 129, 129a, 129b of the Criminal Code; section 20 (1) nos.

  • On the aforesaid basis, Figaro / Wotan would be able to exclude liability in respect of the Regulatory Fine and the Forex Manipulation Claims, since these arise out of forex and/or market manipulation.

  • In this connection, having regard to the natural and ordinary meaning of the Aggregation Wording, the Court is likely to hold that Scarpia is entitled to aggregate the Regulatory Fine, the Forex Manipulation Claims and the Forex Trading Claims, because these claims would likely be considered a single claim “ arising out of or in connection with the same originating cause”, namely, the originating cause of manipulation of the Forex markets.

  • Pursuant to the Justice Ministry's executive provision of 23 October 2015 on "Reporting Obligations in Criminal Proceedings and Proceedings for the Imposition of a Regulatory Fine" (4107- 402.27), all prosecutor's offices in Lower Saxony are also obliged to report to the Justice Ministry of Lower Saxony in criminal matters of extraordinary legal or factual significance.

  • Section 111a of the Copyright Act Regulatory Fine Provisions (1) Any person who, 1.

  • Paul had considered all of the things Lydia was conflicted about at that moment.

  • Regulatory Fine - any civil fine or civil monetary penalty imposed in a regulatory proceeding payable by the Insured to the government entity bringing such regulatory proceeding in such entity’s regulatory or official capacity.

Related to Regulatory Fine

  • 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.

  • Regulatory Filings means any submission to a Regulatory Authority of any appropriate regulatory application together with any related correspondence and documentation, and will include any submission to a regulatory advisory board, marketing authorization application, and any supplement or amendment thereto.

  • Regulatory Materials means, with respect to a Licensed Product for any particular indication in any particular jurisdiction, regulatory applications and submissions (and any supplements or amendments thereto), and any notifications, communications, correspondence, registrations, drug master files, Regulatory Approvals and/or other filings made to, received from or otherwise conducted with a Regulatory Authority, including BLAs and INDs, as applicable, that relate to such Licensed Product in such jurisdiction. Regulatory Materials also include presentations, responses, and applications for Regulatory Approvals.

  • Regulatory Documentation means, with respect to the Compounds, all submissions to Regulatory Authorities in connection with the development of such Compounds, including all INDs and amendments thereto, NDAs and amendments thereto, drug master files, correspondence with regulatory agencies, periodic safety update reports, adverse event files, complaint files, inspection reports and manufacturing records, in each case together with all supporting documents (including documents that include Clinical Data).

  • Regulatory Data means any and all research data, pharmacology data, chemistry, manufacturing, and control data, preclinical data, clinical data or all other documentation submitted, or required to be submitted, to Regulatory Authorities in association with regulatory filings for the Product in the Field (including any Drug Master Files (DMFs), Chemistry, Manufacturing and Control (“CMC”) data, or similar documentation).

  • Regulatory Submissions means all applications, filings, dossiers and the like submitted to a Governmental Authority for the purpose of obtaining Regulatory Approval.

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

  • 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.

  • 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.

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval in a country, territory or possession.

  • Marketing Materials has the meaning ascribed thereto in NI 41-101;

  • Regulatory Documents means the prospectus, annual report, semi-annual report and any other document required under applicable federal securities law to be delivered by the Trust to Fund shareholders.

  • Investigational Product means the Study Drug identified above and the control material, as further detailed in the Protocol;

  • Investigational Medicinal Product means the study drug or control material as defined in the Protocol.

  • Marketing Authorization means all approvals from the relevant Regulatory Authority necessary to market and sell a Product in any country (including without limitation, all applicable pricing and governmental reimbursement approvals even if not legally required to sell Product in a country).

  • Manufacturing Materials means parts, tools, dies, jigs, fixtures, plans, drawings, and information produced or acquired, or rights acquired, specifically to fulfill obligations set forth herein.

  • Promotional Materials means all sales representative training materials and all written, printed, graphic, electronic, audio or video matter, including, without limitation, journal advertisements, sales visual aids, formulary binders, reprints, direct mail, direct-to-consumer advertising, internet postings and sites and broadcast advertisements intended for use or used by either Party or its Affiliates or sublicensees in connection with any promotion of a Product.

  • Commercialization or “Commercialize” means activities directed to marketing, promoting, research and development as required, manufacturing for sale, offering for sale, distributing, importing or selling a product, including sub-licensing or sub-contracting of these activities.

  • Regulatory Authorities means the Commissions and the Exchange;

  • Clinical means having a significant relationship, whether real or potential, direct or indirect, to the actual rendering or outcome of dental care, the practice of dentistry, or the quality of dental care being rendered to a patient;

  • Clinical Studies means human clinical trials for a Licensed Product and any other tests and studies for a Licensed Product in human subjects.

  • Regulatory Approval means any approval or clearance by any governmental agency or agencies having authority to regulate the use or sale of any Licensed Product(s) in the pertinent jurisdiction or territory.

  • Regulatory Approvals means any registrations, licenses, authorizations, permits or approvals issued by any Governmental Authority and applications or submissions related to any of the foregoing.

  • Promotional Material means any communication that relates to the Company or its services made to or directed at, or that relates in any way to the solicitation of a Prospective Customer or a transaction in an Existing Customer’s trading account. Promotional Material includes, but is not limited to, published written texts, training materials, advertisements, market analysis, research reports, correspondence to Existing Customers or Prospective Customers, newsletters and generally anything written that assists in the solicitation process.

  • Clinical Data means the information concerning the safety or performance that is generated from the use of a device and that are sourced from the following:

  • Regulatory entity means any board, commission, agency,