Event Programme definition

Event Programme means the booklet or brochure which contains the Event Schedule and other useful information related to the Event.
Sample 1Sample 2Sample 3

Examples of Event Programme in a sentence

  • The Event Programme shall contain the necessary content according to art.

  • The Organiser shall reproduce the names and logos set out in Exhibit 5 in every communication or promotion related to the Event and the Competi- tions thereof, such as - the official website of the Event; - Event poster(s); - banners or other supports bearing the name of the Event; - the printed Event Programme; - all publications relating to the Event, including press inserts, press re- leases, start and result lists and any other official publication of the Event.

  • The following content shall be published in the Event Programme free of charge at the FIS’ request: - One full colour advertising page in a premium location for use by the World Cup Title Sponsor; - a message to the audience provided by FIS.

  • The cover page of the Event Programme shall bear the official name and logo of the FIS World Cup as well as the name and logo of the FIS in a prominent posi- tion.

Related to Event Programme

  • Programme means any television broadcast and includes-

  • Maintenance Programme shall have the meaning set forth in Clause 14.3; “Maintenance Period” shall have the meaning set forth in Clause 14.1; “Maintenance Requirements” shall have the meaning set forth in Clause 14.2;

  • Phase 2 Clinical Trial means a human clinical trial, for which the primary endpoints include a determination of dose ranges or an indication of efficacy in patients being studied as described in 21 C.F.R. §312.21(b), or an equivalent clinical trial in a country in the Territory other than the United States.

  • Approved program or "approved state" means a state or interstate program that has been approved or authorized by EPA under 40 CFR Part 123 (2000).

  • Phase 1 Clinical Trial means a Clinical Trial of a Product on sufficient numbers of normal volunteers and/or patients that is designed to establish that such Product is safe for its intended use and to support its continued testing in Phase 2 Clinical Trials. For purposes of this Agreement, ‘initiation’ of a Phase 1 Clinical Trial for a Product means the first dosing of such Product in a human subject in a Phase 1 Clinical Trial.