PUBLIKACE A PROPAGACE Sample Clauses

PUBLIKACE A PROPAGACE. Publication 5.1
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PUBLIKACE A PROPAGACE. The Service Provider shall not publish any articles or papers or make any presentations, nor assist any other person in publishing any articles or papers or making any presentations, relating or referring to the Study, the Confidential Information and/or the Intellectual Property, without the prior written consent of PSI and the Sponsor, in their sole discretion.
Sample 1
PUBLIKACE A PROPAGACE. It is understood that the Study is part of a multicenter trial, and Institution may publish, only upon Sponsor’s approval, the results of its part of the Study in collaboration with the other investigators, but in complete compliance with this section and with the Confidential Information section. After the multicenter publication or 12 months after completion of A. Rozumí se, že studie je součástí multicentrického hodnocení a zdravotnické zařízení může se souhlasem zadavatele zveřejnit výsledky své části studie ve spolupráci s ostatními zkoušejícími, avšak zcela v souladu s tímto bodem a s bodem Důvěrné informace. Zdravotnické zařízení může the Study, whichever occurs first, Institution may itself publish the results of its data from the Study. Institution and Principal Investigator shall provide Sponsor and Cmed with an advance copy of any proposed publication or oral presentation at least 60 days prior to the planned date of submission or presentation and Sponsor [and Cmed] shall have 60 days to review the proposed publication for approval and the purposes described below. Sponsor and Cmed may request in writing, and Institution shall, inasmuch as the scientific nature of the publication is not impaired as a result, agree to, (a) the deletion of any Confidential Information, (b) any reasonable changes requested by Sponsor or Cmed, or (c) a delay of such proposed submission for an additional period, not to exceed 180 days, in order to protect its proprietary information and/or Intellectual Property Rights and Know How resulting from the Study. samo zveřejnit výsledky svých údajů ze studie po multicentrické publikaci nebo 12 měsíců od dokončení studie. Zdravotnické zařízení a hlavní zkoušející poskytnou zadavateli a společnosti Cmed předem kopii navrhované publikace nebo ústní prezentace, a to nejméně 60 dnů před plánovaným datem předání nebo prezentace, a zadavatel [a společnost Cmed] budou mít 60 dnů na posouzení navrhované publikace ke schválení a pro níže uvedené důvody. Zadavatel a společnost Cmed mohou písemně požadovat a zdravotnické zařízení bude souhlasit, pokud tím nebude narušena vědecká povaha publikace, s (a) odstraněním všech důvěrných informací, (b) přiměřenými změnami požadovanými zadavatelem nebo společností Cmed, nebo (c) odkladem tohoto navrhovaného předání o další období, které nebude xxxxx xxx 000 xxx, xx účelem ochrany svých chráněných informací nebo práv duševního vlastnictví a know-how, které ze studie vyplývají.
Sample 1
PUBLIKACE A PROPAGACE. It is understood that the Study is part of a multicenter trial, and Healthcare Provider may publish, only upon Sponsor’s approval, the results of its part of the Study in collaboration with the other investigators, but in complete compliance with this section and with the Confidential Information section. After the multicenter publication or 12 months after completion of the Study, whichever occurs first, Healthcare Provider may itself publish the results of its data from the Study. Healthcare Provider and Principal Investigator shall provide Sponsor and Cmed with an advance copy of any proposed publication or oral presentation at least 60 days prior to the planned date of submission or presentation and Sponsor [and Cmed] shall have 60 days to review the proposed publication for A. Rozumí se, že studie je součástí multicentrického hodnocení a poskytovatel zdravotních služeb může se souhlasem zadavatele zveřejnit výsledky své části studie ve spolupráci s ostatními zkoušejícími, avšak zcela v souladu s tímto bodem a s bodem Důvěrné informace. Poskytovatel zdravotních služeb může sám zveřejnit výsledky svých údajů ze studie po multicentrické publikaci nebo 12 měsíců od dokončení studie. Poskytovatel zdravotních služeb a hlavní zkoušející poskytnou zadavateli a společnosti Cmed předem kopii navrhované publikace nebo ústní prezentace, a to nejméně 60 dnů před plánovaným datem předání nebo prezentace, a zadavatel [a společnost Cmed] budou mít 60 dnů na posouzení navrhované publikace ke schválení a pro níže
Sample 1

Related to PUBLIKACE A PROPAGACE

  • Publikace The Institution and the Investigator agree that the Sponsor shall have the sole and exclusive right to the first publication of the results of the Study. Such Sponsor publication is intended to be a multi-center publication of the Study results, collected from all investigators and institutions participating in the Study (the “Multi- Center Publication”). If the Investigator is interested in contributing to or participating in the Multi-Center Publication, he or she must contact the Sponsor. Selection of authors/participants will be governed by the Sponsor, considering individuals’ contribution to the Study.

  • Vaccinations Contractor understands, acknowledges, and agrees that, pursuant to Article II of the General Appropriations Act, none of the General Revenue Funds appropriated to the Department of State Health Services (DSHS) may be used for the purpose of promoting or advertising COVID-19 vaccinations in the 2024-25 biennium. It is also the intent of the legislature that to the extent allowed by federal law, any federal funds allocated to DSHS shall be expended for activities other than promoting or advertising COVID-19 vaccinations. Contractor represents and warrants that it is not ineligible, nor will it be ineligible during the term of this Contract, to receive appropriated funding pursuant to Article II.

  • Hepatitis B Vaccine Where the Hospital identifies high risk areas where employees are exposed to Hepatitis B, the Hospital will provide, at no cost to the employees, a Hepatitis B vaccine.

  • Study An application for leave of absence for professional study must be supported by a written statement indicating what study or research is to be undertaken, or, if applicable, what subjects are to be studied and at what institutions.

  • Originating Switched Access Detail Usage Data A category 1101XX record as defined in the EMI Telcordia Practice BR-010-200- 010.

  • Public Procurement The Parties shall cooperate to develop conditions for open and competitive award of contracts for goods and services in particular through calls for tenders.

  • Vlastnictví Zdravotnické zařízení si ponechá a bude uchovávat Zdravotní záznamy. Zdravotnické zařízení a Zkoušející převedou na Zadavatele veškerá svá práva, nároky a tituly, včetně práv duševního vlastnictví k Důvěrným informacím (ve smyslu níže uvedeném) a k jakýmkoli jiným Studijním datům a údajům.

  • Influenza Vaccine Upon recommendation of the Medical Officer of Health, all employees shall be required, on an annual basis to be vaccinated and or to take antiviral medication for influenza. If the costs of such medication are not covered by some other sources, the Employer will pay the cost for such medication. If the employee fails to take the required medication, she may be placed on an unpaid leave of absence during any influenza outbreak in the home until such time as the employee has been cleared by the public health or the Employer to return to the work environment. The only exception to this would be employees for whom taking the medication will result in the employee being physically ill to the extent that she cannot attend work. Upon written direction from the employee’s physician of such medical condition in consultation with the Employer’s physician, (if requested), the employee will be permitted to access their sick bank, if any, during any outbreak period. If there is a dispute between the physicians, the employee will be placed on unpaid leave. If the employee gets sick as a reaction to the drug and applies for WSIB the Employer will not oppose the application. If an employee is pregnant and her physician believes the pregnancy could be in jeopardy as a result of the influenza inoculation and/or the antiviral medication she shall be eligible for sick leave in circumstances where she is not allowed to attend at work as a result of an outbreak. This clause shall be interpreted in a manner consistent with the Ontario Human Rights Code.

  • SHOP DRAWINGS, PRODUCT DATA AND SAMPLES 4.12.1 Shop Drawings are drawings, diagrams, schedules and other, data specially prepared for the Work by the Contractor or any Subcontractor, manufacturer, supplier or distributor to illustrate some portion of the Work. 4.12.2 Product Data are illustrations, standard schedules, performance charts, instructions, brochures, diagrams and other information furnished by the Contractor to illustrate a material, product or system for some portion of the Work. 4.12.3 Samples are physical examples which illustrate materials, equipment or workmanship and establish standards by which the Work will be judged. 4.12.4 The Contractor shall review, approve and submit, with reasonable promptness and in such sequence as to cause no delay in the Work or in the work of the State or any separate contractor, all Shop Drawings, Product Data and Samples required by the Contract Documents. 4.12.5 By approving and submitting Shop Drawings, Product Data and Samples, the Contractor represents that he / she has determined and verified all materials, field measurements, and field construction criteria related thereto, or will do so, and that he / she has checked and coordinated the information contained within such submittals with the requirements of the Work and of the Contract Documents. 4.12.6 The Contractor shall not be relieved of responsibility for any deviation from the requirements of the Contract Documents by the Architect's approval of Shop Drawings, Product Data or Samples under Subparagraph 2.2.7 of these General Conditions unless the Contractor has specifically informed the Architect and the State in writing of such deviation at the time of sub- mission and the Architect and the State has given written approval to the specific deviation. The Contractor shall not be relieved from responsibility for errors or omissions in the Shop Drawings, Product Data or Samples by the Architect's approval thereof. 4.12.7 The Contractor shall direct specific attention, in writing or on resubmitted Shop Drawings, Product Data or Samples, to revisions other than those requested by the Architect on previous submittals. 4.12.8 No portion of the Work requiring submission of a Shop Drawing, Product Data or Sample shall be commenced until the submittal has been approved by the Architect as provided in Subparagraph 2.2.7 of these General Conditions. All such portions of the Work shall be in accordance with approved submittals.

  • Porcupine Site Highway 11 and the City of Timmins Thunder Bay and District Toronto/York-Peel

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