THE EVENT PROGRAMME Sample Clauses

THE EVENT PROGRAMME. The Organiser shall publish a detailed programme of the entire Event and all Competitions as hard copy and on the website of the Event. The Event Programme shall contain the necessary content according to art. 213 ICR. The following content shall be published in the Event Programme free of charge at 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 FIS in a prominent position. The proposed lay-out and content of the programme shall be submitted to FIS for prior approval, such approval not to be unreasonably withheld or delayed.
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THE EVENT PROGRAMME. The Organiser shall publish a detailed programme of the entire Event and all Compe- titions as hard copy and on the website of the Event. The Event Programme shall contain the necessary content according to art. 213 ICR. 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;
Sample 1Sample 2Sample 3See All (6)
THE EVENT PROGRAMME. The LOC shall publish a detailed programme of the entire Event and all Competitions as hard copy and on the website of the Event. The Event Programme shall contain the necessary content according ISMF “Rules for organizing international ski mountaineering competitions”. The following content shall be published in the Event Programme free of charge at the ISMF’ request: • one full color advertising page in a premium location for use by the World Cup Presenting Sponsor; • one full color advertising page for use by the World Cup Sponsor • one full color advertising page for use by NF • a message to the audience provided by ISMF. The cover page of the Event Programme shall bear the official name and logo of the ISMF World Cup as well as the name and logo of the ISMF in a prominent position. The proposed lay-out and content of the programme shall be submitted to the ISMF Marketing & Communication Department for prior approval, such approval not to be unreasonably withheld or delayed. See the Rules for organizing international ski mountaineering competitions.
Sample 1
THE EVENT PROGRAMME. The Organiser shall publish a detailed programme of the entire Event and all Competitions as hard copy and on the website of the Event. The Event Programme shall contain the necessary content according to art. 213 ICR. The cover page of the Event Programme shall bear the official name and logo of the FIS Grand Prix as well as the name and logo of the FIS in a prominent position. The proposed lay-out and content of the programme shall be submit- xxx to the FIS for prior approval, such approval not to be unreasonably with- held or delayed.
Sample 1
THE EVENT PROGRAMME. The Organiser shall publish a detailed programme of the entire Event and all Competitions as hard copy and on the website of the Event. The Event Programme shall contain the necessary content according to art. 213 ICR. The cover page of the Event Programme shall bear the official name and logo of the FIS Grand Prix as well as the name and logo of the FIS in a prominent position. The proposed lay-out and content of the programme shall be submit- xxx to the FIS for prior approval, such approval not to be unreasonably withheld or delayed.
Sample 1

Related to THE EVENT PROGRAMME

  • Clinical Trials The studies, tests and preclinical and clinical trials conducted by or on behalf of, or sponsored by, the Company, or in which the Company has participated, that are described in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, or the results of which are referred to in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus, were and, if still pending, are being conducted in all material respects in accordance with protocols, procedures and controls pursuant to, where applicable, accepted professional and scientific standards for products or product candidates comparable to those being developed by the Company and all applicable statutes, rules and regulations of the FDA, the EMEA, Health Canada and other comparable drug and medical device (including diagnostic product) regulatory agencies outside of the United States to which they are subject; the descriptions of the results of such studies, tests and trials contained in the Registration Statement, the Time of Sale Disclosure Package or the Prospectus do not contain any misstatement of a material fact or omit a material fact necessary to make such statements not misleading; the Company has no knowledge of any studies, tests or trials not described in the Disclosure Package and the Prospectus the results of which reasonably call into question in any material respect the results of the studies, tests and trials described in the Registration Statement, the Time of Sale Disclosure Package or Prospectus; and the Company has not received any notices or other correspondence from the FDA, EMEA, Health Canada or any other foreign, state or local governmental body exercising comparable authority or any Institutional Review Board or comparable authority requiring or threatening the termination, suspension or material modification of any studies, tests or preclinical or clinical trials conducted by or on behalf of, or sponsored by, the Company or in which the Company has participated, and, to the Company’s knowledge, there are no reasonable grounds for the same. Except as disclosed in the Registration Statement, the Time of Sale Disclosure Package and the Prospectus, there has not been any violation of law or regulation by the Company in its respective product development efforts, submissions or reports to any regulatory authority that could reasonably be expected to require investigation, corrective action or enforcement action.

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