Equivalent authority’ means an authority in respect of which the EU has made a positive equivalence determination according the criteria and procedures specified in Appendix 4 and as referred to in the EU laws, regulations and administrative provisions listed in Appendix 1.
Equivalent authority’ means an authority in respect of which the EU has made a positive equivalence determination according the criteria and procedures specified in
Equivalent authority’ means an entity that carries out duties similar to that of a Board of Directors, for a recipient or subrecipient of FTA funds under 49 U.S.C. Chapter 53, including sufficient authority to review and approve a recipient or subrecipient's Public Transportation Agency Safety Plan.¶
More Definitions of Equivalent authority’
Equivalent authority’ means a position as Principal or Chief Financial Officer or Principal or Chief Accounting Officer or another position in finance or accounting that would require you to report directly to either (i) the Chief Executive Officer or (ii) the audit committee of the Board of Directors. It is further agreed that any position that you are offered with the Company or Successor Enterprise following a Change of Control for which the base salary (on an annual basis) is at least as great your base salary immediately prior to the Change of Control shall be deemed to be a position of Equivalent Authority for purposes of this letter.
Equivalent authority’ means a regulatory authority of a Party that is recognised as an equivalent authority by the other Party;
Equivalent authority’ means an authority recognized by the cabinet and by the U.S. EPA as having a program for certification of vapor recovery systems equivalent to that of CARB.
Equivalent authority’ means a licence or permit under the Community Services Act or a licence for the provision of a child care service in another State or Territory. The term is used in clauses 206, 208 and 209, and catches an applicant whose licence has been cancelled under the Community Services Act or in another State or Territory.
Equivalent authority’ means an entity that carries out duties similar to that of a Board of Directors, for a recipient or subrecipient of FTA funds under 49 U.S.C. Chapter 53, including
Equivalent authority’ means an entity that carries out duties similar to that of a Board of Directors, for a recipient or sub recipient of FTA funds under 49 U.S.C. Chapter 53, including sufficient authority to review and approve a recipient or sub recipient’s Public Transportation Agency Safety Plan.
Equivalent authority’ means an Authority in respect of which Swissmedic has made a positive equivalence determination according to the criteria and procedures specified in Annex 3 and as referred to in the Switzerland laws and regulations listed in Annex 1; Good Manufacturing Practice (GMP) means systems that assure proper design, monitoring, and control of manufacturing processes and facilities, the adherence to which assures the identity, strength, quality, and purity of pharmaceuticals. GMP includes strong quality management systems, obtaining appropriate quality raw materials (including starting materials) and packaging materials, establishing robust operating procedures, detecting and investigating product quality deviations, and maintaining reliable testing laboratories; GMP inspection means an inspection of manufacturing facilities, including processing, packaging, testing, and sterilizing facilities, and contract facilities performing these functions, during the marketing of products for compliance with GMP; Inspection means an on-site evaluation of a manufacturing facility to determine whether the manufacturing facility is operating in compliance with GMP, its commitments made as part of the approval to market a product, or both; Inspection Report means a report written by an investigator or inspector of an Authority concerning an inspection of a manufacturing facility that the investigator or inspector conducted that describes the purpose, scope, and details concerning the coverage of an inspection and includes written observations or factual findings bearing on the manufacturing facility’s conformance to applicable GMP requirements set out in the laws and regulations listed in Annex 1 and any commitments made as part of the approval to market a product; Official GMP document means a document issued by an Authority following an inspection of a manufacturing facility. Examples of official GMP documents include: inspection reports; certificates issued by an authority attesting the compliance of a manufacturing facility with GMP; GMP non-compliance statements issued by Swissmedic; and notices of observation, untitled letters, warning letters, and import alerts issued by FDA; Post-approval inspection means an inspection of a manufacturing facility specific to an approved application; and Pre-approval inspection means an inspection of a manufacturing facility carried out as part of the review of an application before a marketing approval is granted.