Confidential Information A. During and for a period of ten (10) years after the expiration or early termination of this Agreement, Institution and Principal Investigator shall retain in confidence all test articles and proprietary data and/or information obtained from Sponsor or generated pursuant to the Study including, but not limited to, the Protocol, the investigator's brochure, interim results and any other information or material disclosed under confidential disclosure agreements previously entered into between the parties ("Confidential Information"). This restriction shall not apply to Confidential Information that: (i) is or becomes public knowledge (through no fault of Institution or Principal Investigator); or (ii) is lawfully made available to Institution or Principal Investigator by an independent third party owing no obligation of confidentiality to Sponsor with regard thereto (and such lawful right can be properly demonstrated by Institution or Principal Investigator); or (iii) is already in Institution's or Principal Investigator’s possession at the time of receipt from Sponsor (and such prior possession can be properly demonstrated by Institution or Principal Investigator); or (iv) is published in accordance with the express terms of this Agreement. B. Institution may disclose Confidential 8. Náklady a platby Rozpočet pro Studii je připojen jako příloha B a začleněn do této Smlouvy odkazem. Platby stanovené v těchto rozpočtových formulářích jsou stranami této Smlouvy považovány za přiměřenou odměnu za práci provedenou danou stranou. Platby ze strany Zadavatele za služby poskytnuté Zdravotnickým zařízením a Hlavním zkoušejícím na základě této Smlouvy (i) představují přiměřenou tržní hodnotu za takové služby, (ii) byly sjednány jako transakce v běžných obchodních vztazích a (iii) nebyly určeny způsobem, který zohledňuje objem nebo hodnotu jakýchkoliv doporučení nebo jakkoliv jinak generovanou obchodní spolupráci mezi stranami. Za vykonanou práci nebo vynaložené výdaje, za xxx xx Zadavatel povinen provést platbu, nebude Zdravotnické zařízení a Hlavní zkoušející požadovat z jakéhokoliv zdroje dodatečnou úhradu.
Confidential Information A. During and for a period of ten (10) years after the expiration or early termination of this Agreement, Institution and Principal Investigator shall retain in confidence all test articles and proprietary data and/or information obtained from Sponsor or generated pursuant to the Study including, but not limited to, the Protocol, the investigator's brochure, interim results and any other information or material disclosed under confidential disclosure agreements previously entered into between the parties ("Confidential Information"). This restriction shall not apply to Confidential Information that: (i) is or becomes public knowledge (through no fault of Institution or Principal Investigator); or (ii) is lawfully made available to Institution or Principal Investigator by an independent third party owing no obligation of confidentiality to Sponsor with regard thereto (and such lawful right can be properly demonstrated by Institution or Principal Investigator); or (iii) is already in Institution's or Principal Investigator’s possession at the time of receipt from Sponsor (and such prior possession can be properly demonstrated by Institution or Principal Investigator); or (iv) is published in accordance with the express terms of this Agreement. B. Institution may disclose Confidential Information to the extent it is required by law, regulation, rule, act or order of any governmental authority or agency. To permit Sponsor an opportunity to intervene by seeking a protective order or other similar order, in order to limit or prevent disclosures of Confidential Information, Institution or Principal Investigator shall immediately notify Sponsor, in writing, if it is requested by a court order or a governmental authority or agency to disclose Confidential Information in Institution's or Principal Investigator’s possession and thereafter Institution or Principal Investigator shall disclose only the minimum Confidential Information required to be disclosed in order to comply, whether or not a protective order or other similar order is obtained by Sponsor.
C. Subject to applicable legal and regulatory requirements, Institution and Principal Investigator agree to promptly return to Sponsor, upon its request, all Confidential Information obtained from Sponsor or belonging to Sponsor pursuant to this Agreement; provided, however, that Institution's legal counsel may retain one copy of Confidential Information in a secure location for purposes of identifying Institution's o...
Confidential Information A. During and for a period of ten (10) years after the expiration or early termination of this Agreement, Institution and Principal Investigator shall retain in confidence all test articles and proprietary data and/or information obtained from Sponsor or generated pursuant to the Study including, but not limited to, the Protocol, the investigator's brochure, interim results and any other information or material disclosed under confidential disclosure agreements previously entered into between the parties ("Confidential Information"). This restriction shall not apply to Confidential Information that: (i) is or becomes public knowledge (through no fault of Institution or Principal Investigator); or (ii) is lawfully made available to Institution or Principal Investigator by an independent third party owing no obligation of confidentiality to Sponsor with regard thereto (and such lawful right can be properly demonstrated by Institution or Principal Investigator); or dokumentů, které budou předány kterémukoli inspektorovi nebo auditorovi. V případě, že bude FDA nebo jiný regulatorní orgán požadovat přijetí jakéhokoli opatření za účelem řešení jakékoli obsílky, Hlavní zkoušející a Zdravotnické zařízení přijmou po konzultaci se Zadavatelem opatření nezbytné pro řešení takovéto obsílky a souhlasí, že budou spolupracovat se Zadavatelem, pokud jde o jakoukoliv takovou obsílku nebo opatření přijaté v souvislosti s ní.
Confidential Information A. During and for a period of ten (10) years after the expiration or early termination of this Agreement, Institution and Principal Investigator shall retain in confidence all test articles and proprietary data and/or information obtained from Sponsor or generated pursuant to the Study including, but not limited to, the Protocol, the investigator's brochure, interim results and any other information or material disclosed under confidential disclosure agreements previously entered into between the parties ("Confidential Information"). This restriction shall not apply to Confidential Information that: (i) is or becomes public knowledge (through no fault of Institution or Principal Investigator); or (ii) is lawfully made available to Institution or Principal Investigator by an independent third party owing no obligation of confidentiality to Sponsor with regard thereto (and such lawful right can be properly demonstrated by Institution or Principal Investigator); or (iii) is already in Institution's or Principal Investigator’s possession at the time of receipt from Sponsor (and such prior possession can be properly demonstrated by Institution or Principal Investigator); or (iv) is published in accordance with the express terms of this Agreement. B. Institution may disclose Confidential Information to the extent it is required by law, regulation, rule, act or order of any governmental authority or agency. To permit Sponsor an opportunity to intervene by seeking a protective order or other similar order, in order to limit or prevent disclosures of Confidential Information, Institution or Principal Investigator shall immediately notify Sponsor, in writing, if it is requested by a court order or a governmental authority or agency to disclose Confidential Information in vyjádřilo souhlas. Smluvní strany tímto prohlašují, že z jejich strany neexistuje žádný střet zájmů finanční či nefinanční povahy, který by bránil řádné realizaci klinického hodnocení v souladu s obecně platnými právními předpisy a regulatorními požadavky (zejména na správnou klinickou praxi).
Confidential Information A. During and for a period of ten (10) years after the expiration or early termination of this Agreement, Medical service provider and Principal Investigator shall retain in confidence all test articles and proprietary data and/or information obtained from Sponsor or generated pursuant to the Study including, but not limited to, the Protocol, the investigator's brochure, interim results and any other information or material disclosed under confidential disclosure agreements previously entered into between the parties ("Confidential Information"). This restriction shall not apply to Confidential Information that: (i) is or becomes public knowledge (through no fault of Medical service provider or Principal Investigator); or (ii) is lawfully made available to Medical service provider or Principal Investigator by an independent third party owing no obligation of confidentiality to Sponsor with regard thereto (and such lawful right can be properly demonstrated by Medical service provider or Principal Investigator); or (iii) is already in Medical service provider's or Principal Investigator’s possession at the time of receipt from Sponsor (and such prior possession can be properly demonstrated by Medical service provider or Principal Investigator); or (iv) is published in accordance with the express terms of this Agreement. B. Medical service provider may disclose Confidential Information to the extent it is required by law, regulation, rule, act or order of any governmental authority or agency. To permit Sponsor an opportunity to intervene by seeking a protective order or other similar order, in order to limit or prevent disclosures of Confidential Information, Medical service provider or Principal Investigator shall immediately notify Sponsor, in writing, if it is requested by a court order or a governmental authority or agency to disclose Confidential Information in Medical service provider's or Principal Investigator’s possession and thereafter Medical service provider or Principal Investigator shall disclose only the minimum Confidential Information required to be disclosed in order to comply, whether or not a protective order or other similar order is obtained by Sponsor.
Confidential Information A. During and for a period of ten (10) years Zadavatelem, aby řádně napravili nebo se zabývali nedostatky zjištěnými v průběhu jakéhokoliv auditu, a souhlasí, že budou spolupracovat se Zadavatelem, pokud jde o jakékoliv opatření podniknuté za účelem nápravy těchto nedostatků. K. Hlavní zkoušející souhlasí, že upozorní Zadavatele ve lhůtě čtyřiadvaceti (24) hodin v případě, že Státní ústav pro kontrolu léčiv, FDA nebo jakýkoli jiný regulatorní orgán uvědomí místo provádění Studie o připravované inspekci/auditu. Hlavní zkoušející xxxx xxxx Zadavateli zprávu o výsledku inspekce/auditu a to do čtyřiadvaceti (24) hodin od přijetí takové zprávy a umožní Zadavateli spolupracovat na přípravě odpovědi na jakoukoli obsílku. Tyto reakce budou připraveny do dvou (2) týdnů od takové žádosti nebo před touto lhůtou v souladu s požadavkem příslušného regulatorního orgánu. Hlavní zkoušející také poskytne Zadavateli kopie všech dokumentů, které budou předány kterémukoli inspektorovi nebo auditorovi. V případě, že bude FDA nebo jiný regulatorní orgán požadovat přijetí jakéhokoli opatření za účelem řešení jakékoli obsílky, Hlavní zkoušející a Instituce přijmou po konzultaci se Zadavatelem opatření nezbytné pro řešení takovéto obsílky a souhlasí, že budou spolupracovat se Zadavatelem, pokud jde o jakoukoliv takovou obsílku nebo opatření přijaté v souvislosti s ní.
Confidential Information A. The Consultant acknowledges that he will acquire information about certain matters and things which are confidential to the Company ("Confidential Information"), and which information is the exclusive property of the Company including but not limited to the following: i) product design and manufacturing information and computer programs, codes, materials, prototypes, products samples, analyses, reports;
Confidential Information A. The Executive agrees that she shall hold in strict confidence and shall not at any time during or after her employment with the Company, directly or indirectly, (i) reveal, report, publicize, disclose, or transfer any Confidential Information (as described below) or any part thereof to any person or entity, (ii) use any of the Confidential Information or any part thereof for any purpose other than in the course of her duties on behalf of the Company, or (iii) assist any person or entity other than the Company to secure any benefit from the Confidential Information or any part thereof. All Confidential Information (regardless of the medium retained) and all abstracts, summaries or writings based upon or reflecting any Confidential Information in the Executive's possession shall be delivered by the Executive to the Company upon request therefore by the Company or automatically upon the expiration of the Term or termination of this Agreement.
Confidential Information A. In this Agreement “Confidential Information” means information proprietary to the Employer that is not publicly known or available, including but not limited to personnel information, customer information, supplier information, contractor information, pricing information, financial information, marketing information, business opportunities, technology, research and development, manufacturing and information relating to intellectual property, owned, licensed, or used by the Employer or in which the Employer otherwise has an interest, and includes Confidential Information created by the Executive in the course of his employment, jointly or alone. The Executive acknowledges that the Confidential Information is the exclusive property of the Employer.
Confidential Information A. During and for a period of ten (10) years after the expiration or early termination of this Agreement, Institution and Principal Investigator shall retain in confidence all test articles and proprietary data and/or information obtained from Sponsor or generated pursuant to the Study including, but not limited to, the Protocol, the investigator's brochure, interim results and any other information or material disclosed under confidential disclosure agreements previously entered into between the parties ("Confidential Information"). This restriction shall not apply to Confidential Information that: Státní ústav pro kontrolu léčiv, FDA nebo jakýkoli jiný regulatorní orgán uvědomí místo provádění Studie o připravované inspekci/auditu. Hlavní zkoušející xxxx xxxx Zadavateli zprávu o výsledku inspekce/auditu a to do čtyřiadvaceti (24) hodin od přijetí takové zprávy a umožní Zadavateli spolupracovat na přípravě odpovědi na jakoukoli obsílku. Tyto reakce budou připraveny do dvou (2) týdnů od takové žádosti nebo před touto lhůtou v souladu s požadavkem příslušného regulatorního orgánu. Hlavní zkoušející také poskytne Zadavateli kopie všech dokumentů, které budou předány kterémukoli inspektorovi nebo auditorovi. V případě, že bude FDA nebo jiný regulatorní orgán požadovat přijetí jakéhokoli opatření za účelem řešení jakékoli obsílky, Hlavní zkoušející a Zdravotnické zařízení přijmou po konzultaci se Zadavatelem opatření nezbytné pro řešení takovéto obsílky a souhlasí, že budou spolupracovat se Zadavatelem, pokud jde o jakoukoliv takovou obsílku nebo opatření přijaté v souvislosti s ní.
