Rozsah prací Sample Clauses

Rozsah prací a. Principal Investigator shall conduct Study at Institution in accordance with the following provisions, adherence to which shall be supervised by Institution, and shall require sub-investigator(s), and Institution’s other employees, subcontractors and agents performing services related to the Study (collectively, “Institution Personnel”) to conduct the Study in accordance with: (i) this Agreement; (ii) the Protocol; (iii) all written instruction provided by or on behalf of AbbVie; and (iv) all applicable laws and regulations and industry codes of practice (collectively “Law(s)”), including without limitation, anti-bribery and anti- corruption laws, International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use E6 Good Clinical Practice (“ICH-GCP”), the Act on Pharmaceuticals No. 378/2007 Sb., as amended (“Act on Pharmaceuticals”), the Act on Health Care Services No. 372/2011 Sb., as amended (“Health Care Services Law”), Decree No. 226/2008 Sb., as amended,on Good Clinical Practice and Detailed Conditions of Clinical Trials on Medicinal Products, Decree No. 84/2008 Sb. on Good Pharmacy Practice, as amended (“Good Pharmacy Practice”), Decree No. 86/2008 Sb. on Good Laboratory Practice in the Area of Medicines, Act No. 110/2019 Sb. on Processing of Personal Data, the EU General Data Protection Regulation (2016/679) and related data protection laws (“Data Protection Law(s)”)and other data protection and privacy laws, as each may be amended, from time to time. In furtherance of the foregoing obligations, AbbVie shall ensure that the State Institute for Drug Control (“SUKL“)and an Ethics Committee (“EC”) established and constituted in accordance with applicable Laws approves and oversees the conduct of the Study. AbbVie shall notify SUKL and EC of (i) the date and place of commencement of the Study within sixty (60) days from its start in the Czech Republic and (ii) the introduction of substantial amendments to the Protocol as required by applicable regulations. Institution shall cause Principal Investigator to observe the procedures set forth for recording and reporting data as required by applicable regulations. a. Hlavní zkoušející bude ve Zdravotnickém zařízení provádět Studii v souladu s následujícími ustanoveními, na jejichž dodržení bude dohlížet Zdravotnické zařízení, a to i na dodržení ze stranydalších zkoušejících a dalších zaměstnancích, subdodavatelích a zástupcích Zdravotnického zařízení spoje...
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Rozsah prací. Studijní pracoviště a hlavní zkoušející souhlasí s tím, že budou provádět tuto studii v souladu s protokolem založeném na použití hodnoceného přípravku, jak je popsáno v souboru informací pro zkoušejícího. V rozsahu, v němž se některé podmínky protokolu mohou lišit od podmínek této smlouvy, bude se chování smluvních stran řídit podmínkami smlouvy.
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Rozsah prací a. Institution and Principal Investigator each shall conduct and require, sub-investigator(s), and Institution’s other employees, subcontractors and agents performing services related to the Study (collectively, “Study Personnel”) to conduct the Study in accordance with: (i) this Agreement; (ii) the Protocol; (iii) all written instruction provided by or on a. Zdravotnické zařízení a Hlavní zkoušející budou provádět Studii v souladu s následujícími ustanoveními, jejichž dodržení budou vyžadovat i na dalších zkoušejících a dalších zaměstnancích, subdodavatelích a zástupcích Zdravotnického zařízení spojených se Studií (společně „Studijní Personál“). Studie se bude provádět v souladu s (i)
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Rozsah prací a. The Provider shall conduct and shall require Principal Investigator, subinvestigator(s), and the Provider’s other employees, subcontractors and agents performing services related to the Study (collectively, the “Provider’s Personnel”) to conduct the Study in accordance with: (i) this Agreement; (ii) the Protocol; (iii) all written instruction provided by or on behalf of AbbVie; and (iv) all applicable laws and regulations and industry codes of practice (collectively “Law(s)”), including without limitation, anti-bribery and anti- corruption laws, International Conference on a Poskytovatel bude provádět Studii a bude vyžadovat, aby Hlavní zkoušející, další zkoušející a ostatní zaměstnanci Poskytovatelem, subdodavatelé a zástupci poskytující služby související se Studií (společně „Personál Poskytovatele“) Studii prováděli v souladu s: (i) touto Smlouvou, (ii) Protokolem, (iii) všemi písemnými pokyny poskytnutými společností AbbVie nebo jejím jménem; a
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Rozsah prací a. Institution and Principal Investigator each shall conduct and require, subinvestigator(s), and Institution’s other employees, subcontractors and agents performing services related to the Study (collectively, “Institution Personnel”) to conduct the Study in accordance with: (i) this Agreement; (ii) the Protocol; (iii) all written instruction provided by or on behalf of AbbVie; and (iv) all applicable laws and regulations and industry codes of practice (collectively “Law(s)”), including without limitation, anti-bribery and anti-corruption laws, International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use E6 Good Clinical Practice (“ICH-GCP”), the Act on Pharmaceuticals No. 378/2007 Sb., as amended (“Act on Pharmaceuticals”), the Act on Health Care Services No. 372/2011 Sb., as amended (“Health a. Zdravotnické zařízení a Hlavní zkoušející budou provádět Studii v souladu s následujícími ustanoveními, jejichž dodržení budou vyžadovat i na dalších zkoušejících a dalších zaměstnancích, subdodavatelích a zástupcích Zdravotnického zařízení spojených se Studií (společně „Personál zdravotnického zařízení“). Studie se bude provádět v souladu s (i) touto Smlouvou, (ii) Protokolem, (iii) všemi písemnými pokyny poskytnutými společností AbbVie nebo jejím jménem; a
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Rozsah prací a. Provider of Medical Services and Principal Investigator each shall conduct and require, subinvestigator(s), and Provider of Medical Services’ other employees, subcontractors and agents performing services related to the Study (collectively, “Provider of Medical Services Personnel”) to a. Poskytovatel zdravotních služeb a Hlavní zkoušející budou provádět Studii v souladu s následujícími ustanoveními, jejichž dodržení budou vyžadovat i na dalších zkoušejících a dalších zaměstnancích, subdodavatelích a zástupcích Poskytovatele zdravotních služeb spojených se Studií (společně
Sample 1
Rozsah prací a. Institution and Principal Investigator each shall conduct and require, subinvestigator(s), and Institution’s other employees, subcontractors and agents performing services related to the Study (collectively, “Study Personnel”) to conduct the Study in accordance with: (i) this Agreement; (ii) the Protocol; (iii) all written instruction provided by or on behalf of AbbVie; and (iv) all applicable laws and regulations and industry codes of practice binding in a. Zdravotnické zařízení a Hlavní zkoušející budou provádět Studii v souladu s následujícími ustanoveními, jejichž dodržení budou vyžadovat i na dalších zkoušejících a dalších zaměstnancích, subdodavatelích a zástupcích Zdravotnického zařízení spojených se Studií (společně „Studijní Personál“). Studie se bude provádět v souladu s (i) touto Smlouvou, (ii) Protokolem, (iii) všemi písemnými pokyny poskytnutými společností AbbVie nebo jejím
Sample 1
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Rozsah prací a. Institution and Principal Investigator each shall conduct and require, sub-investigator(s), and Institution’s other employees, subcontractors and agents performing services related to the Study (collectively, “Study Personnel”) to conduct the Study in accordance with: (i) this Agreement; (ii) the Protocol; (iii) all written instruction provided by or on behalf of AbbVie; and (iv) all applicable laws and regulations and industry codes of practice applicable in Czech Republic (collectively “Law(s)”), including without limitation, anti-bribery and anti-corruption laws, International Conference on Harmonization of a. Zdravotnické zařízení a Hlavní zkoušející budou provádět Studii v souladu s následujícími ustanoveními, jejichž dodržení budou vyžadovat i na dalších zkoušejících a dalších zaměstnancích, subdodavatelích a zástupcích Zdravotnického zařízení spojených se Studií (společně „Studijní personál“). Studie se bude provádět v souladu s (i) touto Smlouvou, (ii) Protokolem, (iii) všemi písemnými pokyny poskytnutými společností AbbVie nebo jejím jménem; a
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  • DUŠEVNÍ VLASTNICTVÍ a) The Institution and the Investigator acknowledge and agree that the Sponsor shall have exclusive ownership rights to all Study Data, Study results, information, improvements, developments, discoveries, inventions, work, know-how and other rights (whether or not patentable), created, developed, and/or reduced to practice as a result of or in connection with the conduct of the Study and/or the use of the Study Drug or the Confidential Information, together with all intellectual property rights (existing and future) relating thereto (“Intellectual Property”) conceived by the Institution or the Investigator or Study Personnel, solely or jointly with others as a result of work done under this Agreement, to the widest extent possible under applicable law. The Institution and the Investigator shall promptly disclose in writing to PSI and the Sponsor all Intellectual Property made or reduced to practice by the Institution, the Investigator and/or the Study Personnel related to the Study. At the Sponsor's request, the Institution and the Investigator shall cause all rights titles and interests in and to any such Intellectual Property to be assigned to the Sponsor without additional compensation and provide reasonable assistance to obtain patents, including causing the execution of any invention assignment or other documents. b) All parties to this Agreement and Sponsor shall retain all right, title and interest in any Intellectual Property that was owned by such party or Sponsor prior to or apart from the commencement of this Agreement. No a) Zdravotnické zařízení a Hlavní zkoušející uznávají a souhlasí, že Zadavatel bude mít výhradní vlastnická práva ke všem Studijním údajům, výsledkům Studie, informacím, vylepšením, na vývoj, k objevům, vynálezům, dílům, know-how a dalším právům (ať už patentovatelným či nikoli), vytvořeným, vyvinutým, a/nebo uvedeným do praxe v důsledku nebo v souvislosti s prováděním Studie, a/nebo používáním Studijního léku nebo Důvěrných informací společně s právy duševního vlastnictví (stávajícími i budoucími) s nimi souvisejícími (dále jen „Duševní vlastnictví“), které vytvořilo Zdravotnické zařízení, Hlavní zkoušející nebo Studijní personál, samostatně nebo společně s ostatními jako výsledek práce prováděné na základě této Smlouvy, a to v největším možném rozsahu povoleném příslušnými zákonnými předpisy. Zdravotnické zařízení a Hlavní zkoušející budou neprodleně písemně informovat PSI a Zadavatele o veškerém Duševním vlastnictví vytvořeném nebo uvedeném do praxe Zdravotnickým zařízením, Hlavním zkoušejícím a/nebo Studijním personálem v souvislosti se Studií. Na žádost Zadavatele zajistí Zdravotnické zařízení a Hlavní zkoušející převod veškerých práv a zájmů týkajících se Duševního vlastnictví na Zadavatele bez další odměny a poskytnou přiměřenou součinnost k získání patentu včetně zajištění podpisu dokumentů k převodu objevu nebo jiných dokumentů. b) Všechny strany této Smlouvy a Zadavatel si i nadále ponechají veškerá práva, nároky a podíly na jakémkoli Duševním vlastnictví, které daná strana nebo Zadavatel vlastnili před začátkem platnosti této Smlouvy nebo na které license grant or assignment, express or implied, by estoppel or otherwise, is intended by, or shall be inferred from, this Agreement except to the extent necessary for each party to fulfill its obligations under this Agreement or otherwise give effect to this Agreement.

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