Health Authorities definition

Health Authorities means the Governmental Entities which administer Health Laws including the FDA.
Health Authorities means the Governmental Entities which administer Health Laws, including the FDA.
Health Authorities mean all regulatory authorities having jurisdiction over the development, manufacture, use and/or sale of the Product in the Territory, including but not limited to the European Medicines Agency (“EMA”), U.S. Food and Drug Administration (“FDA”) and Health Canada.

Examples of Health Authorities in a sentence

  • The Health Authorities and Providence Health Care agree to provide to employees violence prevention training based on the program that was designed by the Provincial Violence Prevention Steering Committee.

  • If they are fit enough to leave the project and arrive home safely, they should go home and follow the Public Health Authorities instructions for reporting self - isolating and treatment.

  • For purposes of this program, acute care employer includes the following employers: the IWK Health Centre and all District Health Authorities.

  • The Government will ensure that Health Authorities comply with this Agreement and the Physician Master Subsidiary Agreements.

  • The four Health Authorities whose dovetailed seniority lists are less than authority wide may nonetheless choose to offer unfilled vacancies to displaced employees on an authority wide basis.


More Definitions of Health Authorities

Health Authorities means any regulatory authority responsible for regulating the manufacture, marketing, sale and distribution of finished drug products or medicinal products and health care products for human use in the TERRITORY.
Health Authorities has the meaning specified in Section 3.30(a) hereof.
Health Authorities means any national or international health authority including but not limited to those of the European Union, Japan, and the United States.
Health Authorities means (i) with respect to the United States, the FDA, DEA, and United States Department of Health and Human Services, (ii) with respect to Canada, Health Canada, its branches, agencies and secretariats, Agriculture and Agri-Food Canada, its branches, agencies and secretariats, including the Canadian Food Inspection Agency and provincial and local health authorities and any publicly-owned hospitals, (iii) with respect to Mexico, the Mexican Ministry of Health (Secretaría de Salud), COFEPRIS (Comisión Federal para la Protección contra Riesgos Sanitarios), Federal Consumer Protection Agency (Procuraduría Federal del Consumidor), the Ley General de Salud and the Mexican Official Standards (Normas Oficiales Mexicanas), and any publicly-owned hospitals, (iv) with respect to The Netherlands, Ministerie van Volksgezondheid, Welzijn en Sport, College ter Beoordeling van Geneesmiddelen, Inspectie voor de Gezondheidszorg, Stichting Keuringsraad Openbare Aanprijzing Geneesmiddelen, Stichting Keuringsraad Aanprijzing Gezondheidsproducten, Nederlandse Voedsel en Waren Autoriteit, and any publicly-owned hospitals and (v) any government agency having similar authority, power or mandate as one of the aforementioned authorities, in any other jurisdictions where any products of the Banner Companies are investigated, tested, manufactured, transported, promoted, marketed, advertised, imported, exported, distributed or sold.
Health Authorities means the competent National Health Authorities in the TERRITORY.
Health Authorities means the relevant governmental or regulatory entity in the Territory which is authorized to approve/reject Marketing Authorization applications.
Health Authorities means any applicable federal, state or local government authority, quasi-governmental authority, regulatory or administrative agency, authority, body, court, commission or tribunal in the relevant country/ies in the Territory or in the country of manufacture of the Product with jurisdiction or authority in such country over the development, manufacture, supply, storage, import, export, marketing, sale or commercialization (including approval of Marketing Authorizations) and/or reimbursement of pharmaceutical products, including [the FDA] [the UK Medicines and Healthcare Products Regulatory Agency][the Bundesinstitut für Arzneimittel und Medizinprodukte] [the European Medicines Agency].