Regulatory fines and penalties definition

Regulatory fines and penalties means those sums any Insured is required to pay as part of the settlement or judgment of a Privacy Regulatory Action to which this insurance applies.
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Regulatory fines and penalties means any administrative fines and penalties an Insured is legally required to pay because of a claim covered under Coverage 3.
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Regulatory fines and penalties means any civil fines and penalties imposed against an insured as a result of a government investigation.
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Examples of Regulatory fines and penalties in a sentence

  • Regulatory fines and penalties means civil or administrative fines and penalties imposed against an insured in a government investigation.

  • Regulatory fines and penalties are also common when a breach has occurred.Ponemon Institute’s latest report estimates that, “$154 is the cost per lost or stolen record.

  • We have however not made the detailed examination of the cost records with a view to determine whether they are accurate or complete.

  • Regulatory fines and penalties are being much more frequently levied for violations, often involving a number of regulatory agencies who take action for the same or similar issues.

  • Regulatory fines and penalties means civil or administrative fines and penalties imposed against an insuredas a result of a government investigation.Regulatory fines and penalties does not include: A.

  • In addition, background demographics of students, teachers and support personnel will be collected including information about students seeking and gaining admission to IB programs, retention of students and teachers in IB coursework, and recruitment strategies.

  • The responsibility for designating the picketing area vested in the local management, “in consultation with the local Convenor”.

  • Potential business impacts on security incidents can include: > Lost IP> Business interruption> Regulatory fines and penalties> Legal and PR fees> Remediation costs> Reputation AICPA has recently developed a cybersecurity risk management reporting framework that includes a new System and Organization Controls (SOC) for Cybersecurity engagement, through which the enterprise-wide cybersecurity risk management program is reviewed.

  • Regulatory fines and penalties will include such amounts imposed by the Business Conduct Committee and/or the Board, but not late charges or interest charged.

  • Regulatory fines and penalties imposed upon Heinz or ADC shall be paid by Heinz by the date on which the payment is due.


More Definitions of Regulatory fines and penalties

Regulatory fines and penalties means civil fines, civil monetary penalties, or amounts deposited into a consumer redress fund, imposed in a Regulatory Proceeding, but only to the extent they are insurable.
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Regulatory fines and penalties means civil fines or civil monetary penalties imposed for a breach of anydata protection law by a government agency, or governmental licensing or regulatory organisation, pursuant to an order resulting from a Regulatory Claim, but only to the extent they are insurable; provided, that Regulatory Fines and Penalties do not include fines or penalties imposed by any private or industry association regulatory organisation.
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Regulatory fines and penalties means civil fines or penalties imposed by a Regulatory Authority against an Insured as a result of a Privacy Regulatory Proceeding. “Regulatory Fines and Penalties” does not include any amounts deemed uninsurable under the law pursuant to which this Policy is construed, criminal fines or penalties of any nature or PCI DSS Fines and Assessments.
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Regulatory fines and penalties means those sums any Insured is required to pay as part of the settlement or judgment of a Privacy Regulatory Action to which this insurance applies.Z Regulatory Restitution means sums deposited into a fund for the purpose of providing compensation to individuals affected by a Privacy Breach as part of a settlement or judgment resulting from a Privacy Regulatory Action.AA. Security Event means any of the following arising from a Wrongful Act taking place on or after the Retroactive Date, if any, shown in Item 8 of the Declarations:
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Regulatory fines and penalties means those administrative, non-criminal fines or penalties an Insured becomes legally obligated to pay as a result of a covered regulatory violation claim or billing practices claim.
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Related to Regulatory fines and penalties

  • Published Penalties means any additional published cancellation penalties levied by Your travel agency or Travel Supplier that apply to all clients of the travel agency or Travel Supplier and can be documented at time of Your purchase of Travel Arrangements from Your travel agency. The maximum amount reimbursable for travel agency published penalties is 25% of the total trip cost excluding taxes and other non-commissionable items.

  • Regulatory Submissions means any filing, application, or submission with any Regulatory Authority, including authorizations, approvals or clearances arising from the foregoing, including Regulatory Approvals, and all correspondence or communication with or from the relevant Regulatory Authority, as well as minutes of any material meetings, telephone conferences or discussions with the relevant Regulatory Authority, in each case, with respect to a Licensed Product.

  • PAGA Penalties means the total amount of PAGA civil penalties to be paid from the Gross Settlement Amount, allocated seventy-five percent (75%) to the LWDA and the twenty-five percent (25%) to the Aggrieved Employees in settlement of PAGA claims.

  • Regulatory Filing means any approvals, licenses, registrations, submissions and authorizations, and applications therefor, including IND, NDA, BLA, drug dossier or drug master file filed, or Marketing Approval obtained, with respect to an Option Product, Licensed Product or Companion Diagnostic, as applicable, in the Field, including all amendments, supplements, annual reports and the like thereof or therefor filed with or otherwise provided to the applicable Regulatory Authority.

  • 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.

  • CAISO Penalties means any fees, liabilities, assessments, or similar charges assessed by the CAISO for (a) violation of the CAISO Tariff and all applicable protocols, WECC rules or CAISO operating instructions or orders or (b) as a result of Seller’s failure to follow Prudent Electrical Practices. “CAISO Penalties” do not include the costs and charges related to Scheduling and imbalances as addressed in Section 14.1 of this Agreement.

  • Statutory Penalties are those amounts awarded as a penalty, but are fixed in amount by statute.

  • Adverse drug reaction means any undesirable or unexpected medication related event that requires discontinuing a medication or modifying the dose, requires or prolongs hospitalization, results in disability, requires supportive treatment, is life-threatening or results in death, results in congenital anomalies, or occurs following vaccination.

  • Regulatory Approval Application means an application to seek regular or expedited Regulatory Approval of the Licensed Product for sale or marketing in any country(ies) or Region(s) in the Territory, as defined in the applicable Laws and filed with the Regulatory Authority of such country(ies) or Region(s).

  • 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.

  • Regulatory Materials means regulatory applications, submissions, notifications, registrations, or other filings made to or with a Regulatory Authority that are necessary or reasonably desirable in order to develop, manufacture, market, sell or otherwise commercialize a product in a particular country or regulatory jurisdiction. Regulatory Materials include INDs, XXXx and NDAs (as applications, but not the approvals with respect thereto).

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

  • Marketing Authorization Application or “MAA” means an application to the appropriate Regulatory Authority for approval to sell the Product (but excluding Pricing Approval) in any particular country or regulatory jurisdiction.

  • IND means (i) an investigational new drug application filed with the FDA for authorization to commence clinical studies and its equivalent in other countries or regulatory jurisdictions and (ii) all supplements and amendments that may be filed with respect to the foregoing.

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

  • IDEQ means the Idaho Department of Environmental Quality.

  • 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.

  • Regulatory Documentation means all applications, registrations, licenses, authorizations and approvals (including all Approvals), all correspondence submitted to or received from Regulatory Authorities (including minutes and official contact reports relating to any communications with any Regulatory Authority), all supporting documents and all Clinical Trials and tests, including the manufacturing batch records, relating to a Product, and all data contained in any of the foregoing, including all regulatory drug lists, advertising and promotion documents, adverse event files and complaint files.

  • Regulatory Conditions means the conditions set out in paragraphs 3.3 to 3.5 (inclusive) of Part A of Appendix I to the Announcement;

  • BLA means a Biologics License Application under the United States’ Public Health Services Act and Federal Food, Drug and Cosmetics Act, each as amended, and the regulations promulgated thereunder, or a comparable filing seeking Regulatory Approval in any country.

  • FDA means the United States Food and Drug Administration.

  • 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.

  • national regulatory authority means the body or bodies charged by a Member State with any of the regulatory tasks assigned in this Directive and the Specific Directives;

  • Regulatory Approvals with respect to the Warrantholder, means, to the extent applicable and required to permit the Warrantholder to exercise this Warrant for shares of Common Stock and to own such Common Stock without the Warrantholder being in violation of applicable law, rule or regulation, the receipt of any necessary approvals and authorizations of, filings and registrations with, notifications to, or expiration or termination of any applicable waiting period under, the Xxxx-Xxxxx-Xxxxxx Antitrust Improvements Act of 1976, as amended, and the rules and regulations thereunder.

  • MHLW means the Ministry of Health, Labour and Welfare of Japan, or the successor thereto.

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.