LIST OF AUTHORITIES Sample Clauses

LIST OF AUTHORITIES. UNITED STATES Country For medicinal products for human use For medicinal products for veterinary use Austria Austrian Agency for Health and Food Safety/Österreichische Agentur für Gesundheit und Ernährungssicherheit GmbH See responsible authority for human medicinal products Belgium Federal agency for medicines and health products/Federaal Agentschap voor geneesmiddelen en gezondheid- sproducten/Agence fédérale des médi- caments et produits de santé See responsible authority for human medicinal products Bulgaria Bulgarian Drug Agency/ ИЗПЪЛНИТЕЛНА АГЕНЦИЯ ПО ЛЕКАРСТВАТА Bulgarian Food Safety Agency/Българска агенция по безопасност на храните Cyprus Ministry of Health — Pharmaceutical Services/Φαρμακευτικές Υπηρεσίες, Υπουργείο Υγείας Ministry of Agriculture, Rural Develop- ment and Environment-Veterinary Services/Κτηνιατρικές Υπηρεσίες- Υπουργείο Γεωργίας, Αγροτικής Ανάπτυξης και Περιβάλλοντος Czech Republic State Institute for Drug Control/Státní ústav pro kontrolu léčiv (SÚKL) Institute for State Control of Veterinary Biologicals and Medicaments/Ústav pro státní kontrolu veterinárních biopreparátů a léčiv (ÚSKVBL) Croatia Agency for Medicinal Products and Medical Devices/Agencija za lijekove i medicinske proizvode (HALMED) Ministry of Agriculture, Veterinary and Food Safety Directorate/Ministarstvo Poljoprivrede, Uprava za veterinarstvo i sigurnost hrane Denmark Danish Medicines Agency/Laegemid- delstyrelsen See responsible authority for human medicinal products Germany Federal Institute for Drugs and Medical Devices/Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM) Federal Office for Consumer Protection and Food Safety/Bundesamt für Verbrau- cherschutz und Lebensmittelsicherheit (BVL) Xxxx-Xxxxxxx-Institute (PEI), Federal Institute for Vaccines and Biomedi- cines/Xxxx-Xxxxxxx-Institut (PEI) Bundesinstitut für Impfstoffe und biomedizinische Arzneimittel Federal Ministry of Food and Agriculture, Bundesministerium für Ernährung und Landwirtschaft Federal Ministry of Health/Bundes- ministerium für Gesundheit (BMG)/ Zentralstelle der Länder für Gesund- heitsschutz bei Arzneimitteln und Medizinprodukten (ZLG) (1) The Food and Drug Administration EUROPEAN UNION ▼M30 Country For medicinal products for human use For medicinal products for veterinary use Estonia State Agency of Medicines/Ravi- miamet See responsible authority for human medicinal products Greece National Organisation for Medicines/ Ethnikos Organismos Farmakon (EOF) — (ΕΘΝΙΚΟΣ ΟΡΓΑΝΙΣΜΟΣ...
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LIST OF AUTHORITIES. Legislation Income Tax Act, RSC 1985, c 1 (5th supplement), as amended s. 149.1
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LIST OF AUTHORITIES. UNITED STATES: In the United States, the regulatory authority is the Food and Drug Administration.
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Related to LIST OF AUTHORITIES

  • Scope of Authority Committee meetings will be used for communications between the parties, to share information and to address concerns. The committee will have no authority to conduct any negotiations or modify any provision of this Agreement. The committee’s activities and discussions will not be subject to the grievance procedure in Article 30.

  • Lines of Authority The Owner shall establish and maintain lines of authority for his personnel and shall provide this definition to the Construction Manager and all other affected parties.

  • Certification of Authority The undersigned certify that the persons executing this agreement on behalf of City and SDA have legal authority to enter into this agreement on behalf of City and SDA respectively and have full authority to bind City and SDA in a valid Agreement on the terms herein.

  • EXTENT OF AUTHORITY may manage a work area; • exercise a degree of autonomy (advice available on complex or unusual matters); • manage significant projects and/or functions and/or works programmes.

  • Evidence of Authority The Custodian shall be protected in acting upon any instructions, notice, request, consent, certificate or other instrument or paper believed by it to be genuine and to have been properly executed by or on behalf of the Fund. The Custodian may receive and accept a certified copy of a vote of the Board of Directors of the Fund as conclusive evidence (a) of the authority of any person to act in accordance with such vote or (b) of any determination or of any action by the Board of Directors pursuant to the Articles of Incorporation as described in such vote, and such vote may be considered as in full force and effect until receipt by the Custodian of written notice to the contrary.

  • Grant of Authority As of the Effective Date, GlobalSign hereby grants to Subscriber the authority for the term set forth in Section 7 to use the enclosed Digital Certificate to create Digital Signatures or to use the Digital Certificate in conjunction with Private Key or Public Key operations.

  • Reservation of Authority Nothing in this subpart shall limit the authority of the Secretary to take action to enforce conditions or violations of law, including actions necessary to prevent evasions of this subpart.

  • Proof of Authority Buyer shall provide such proof of authority and authorization to enter into this Agreement and the transactions contemplated hereby, and such proof of the power and authority of the individual(s) executing or delivering any documents or certificates on behalf of Buyer as may be reasonably required by Title Company.

  • CERTIFICATE OF AUTHORITY The Trust, the Adviser and the Sub-Adviser shall furnish to each other from time to time certified copies of the resolutions of their Boards of Trustees/Directors or executive committees, as the case may be, evidencing the authority of officers and employees who are authorized to act on behalf of the Trust, a Fund Account, the Adviser and/or the Sub-Adviser.

  • Proof of Authorization 5.3.1 Each Party shall be responsible for obtaining and maintaining Proof of Authorization (POA) as required by applicable federal and state law, as amended from time to time.

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