ISO Requirements definition

ISO Requirements means all rules, regulations and directives issued, enacted or promulgated by the International Organization for Standardization, as amended, as from time to time in effect for medical devices (currently ISO 13485:2003).
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ISO Requirements means the applicable Operating Guides, Metering Guidelines, ISO Generation Interconnection Procedures, Protocols as well as any other documents adopted by the ISO relating to the interconnection and operation of generators and transmission systems in the ISO as amended from time to time, and any successors thereto.
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Examples of ISO Requirements in a sentence

  • Accordingly, the provisions of the Plan shall, with respect to Incentive Stock Options as to the ISO Requirements and with respect to all Options as to the California Securities Requirements, be interpreted and construed in such manner as shall ensure compliance with the ISO Requirements and the California Securities Requirements, respectively, but otherwise grant maximum authority and discretion in all respects to the Board in administering the Plan.

  • This Plan and the grant of Options hereunder is subject to approval by the shareholders of the Company to the extent required by the ISO Requirements and the California Securities Requirements.

  • No event has occurred and no circumstances exist, and the Seller has not received notice regarding any circumstance or condition, that (with or without the passage of time or the giving of notice) may result in a violation of, conflict with or failure to conduct the Diagnostic Business in compliance with said Business Authorizations, ISO Requirements and European Directive.

  • No event has occurred and to Seller’s Knowledge no circumstances exists, and no member of the Seller Group has received notice alleging any circumstance or condition that (with or without the passage of time or the giving of notice) may result in a violation of, conflict with or failure to conduct the Business in compliance with, any applicable Law, FDA Regulation, FDA Authorizations and ISO Requirements.

  • All manufacturing facilities Related to the Business are operated, and Books and Records maintained, in compliance with applicable FDA Regulations and ISO Requirements.