Obligations of Institution. Institution agrees to ensure that Research Staff are informed of and agree to abide by all terms of this Agreement applicable to the activities they perform. Institution agrees to assume all those responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards including, without limitation, all orders and directives of competent public administration authorities, health insurance companies and ethics committees, if any, including, without limitation, all relevant International Conference on Harmonization Good Clinical Practice (“ICH GCP”) guidelines and standards and the World Medical Association Declaration of Helsinki “Ethical Principles for Medical Research Involving Human Subjects” (2013), all applicable laws and guidance relating to clinical studies of medicines, all applicable laws relating to human rights, supply of medicines legislation, legislation relating to human tissue and biological samples, and all applicable laws relating to the confidentiality, privacy and security of Study Subject information including but not limited to the EU General Data Protection Regulation - (EU 2016/679) (“Applicable Law”). Institution agrees to perform Study in accordance with general terms and conditions Odmenu pre skúšajúceho a jeho tím sa zadávateľ zaväzuje riešiť v separátnej zmluve. Laboratórne vyšetrenia ku klinickému skúšaniu budú vykonávané v centrálnych laboratóriách. Zadávateľ sa zaväzuje, že vykonávanie laboratórnych vyšetrení ku klinickej štúdii si zabezpečí osobitnými zmluvami s príslušnými laboratóriami. 1.2. Pomocní skúšajúci a výskumní pracovníci. Zodpovedný skúšajúci môže delegovať povinnosti a zodpovednosti na pomocných skúšajúcich alebo výskumných pracovníkov (pomocný skúšajúci a výskumní pracovníci spoločne označovaní ako „výskumní pracovníci“), ktorí môžu byť zamestnancami alebo zmluvnými tretími stranami len v rozsahu povolenom platnými zákonmi (ďalej definované), ktoré upravujú vykonávanie skúšania, ako je opísané nižšie. Zodpovedný skúšajúci musí spĺňať požiadavky medzinárodnej konferencie o harmonizácii E6 R2, časti 4.2.5 a 4.2.6 a súhlasí s tým, že bude zodpovedný za dohľad nad výskumnými pracovníkmi. Inštitúcia berie na vedomie, že zodpovedný skúšajúci zabezpečí, že pri vykonávaní skúšania budú pomáhať iba jednotlivci, ktorí sú primerane kvalifikovaní a vyškolení, zabezpečí integritu vykonávaných úloh a funkcií súvisiacich so skúšaním a všetkých údajov zo skúšania vytvorených výskumnými pracovníkmi. 1.3.
Obligations of Institution a) Institution agrees that its Cooperating Staff will devote their best efforts to accurately and efficiently perform the work required under this Agreement, which efforts shall include but are not limited to items a) through f) in paragraph 1 of this Article,
Obligations of Institution. 1. Institution will make graduates aware of the articulation and scholarship opportunities by sharing and/or posting information for graduates to review, and will highlight the collaboration and education benefits of WGU through its standard internal communication channels (such as newsletters) with faculty, staff, students.
Obligations of Institution a) Institution agrees that Research Staff will devote their best efforts to accurately and efficiently perform the work required under this Agreement, which efforts shall include but are not limited to items a) through f) in paragraph 1 of this Article,
Obligations of Institution. Institution is responsible to INC Research for compliance by all Trial personnel with the terms of this Agreement. Institution will ensure that any personnel who assist in the conduct of the Trial are informed of and agree to abide by applicable terms of this Agreement. Institution will assume all those responsibilities assigned to clinical study sites under all applicable legal regulations, including without limitation all relevant International Conference on Harmonization Good Clinical Practice (“ICH GCP”) guidelines and standards, applicable Community law, and all applicable laws relating to the confidentiality, privacy and security of patient information ("Applicable Law"). 1.3
Obligations of Institution. Institution and Principal Investigator agree to use their best efforts to conduct the Trial in accordance with the Protocol and all Applicable Laws (as defined below). Institution shall ensure that Research Staff is informed of, and agree to abide by, all terms of this Agreement applicable to the activities they perform. Institution will assume all responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards including, without limitation, all relevant International Conference on Harmonization Good Clinical Practice (“ICH GCP”) guidelines and standards and the World Medical Association Declaration of Helsinki “Ethical Principles for Medical Research Involving Human Subjects” (2013), all applicable laws and guidance relating to clinical trials of medicines and all applicable laws relating to human rights, supply of medicines legislation, legislation relating to human tissue and biological samples, and all applicable laws relating to the 1. Zkoušející a výzkumný personál. 1.1.
Obligations of Institution. Institution will ensure that Research Staff is informed of and agree to abide by all terms of this Agreement applicable to the activities they perform. Institution will assume all those responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards including, without limitation, all relevant International Conference on Harmonization Good Clinical Practice (“ICH GCP”) guidelines and standards and the World Medical Association Declaration of Helsinki “Ethical Principles for Medical Research Involving Human Subjects” (2013), all applicable laws and guidance relating to clinical trials of medicines and all applicable laws relating to human rights, supply of medicines legislation, legislation relating to human tissue and biological samples, and all applicable laws relating to the confidentiality, privacy and security of Trial Subject information inclusive but not limited to the EU General Data Protection Regulation – GDPR (“Applicable Law”). 1.3.
Obligations of Institution. 5.1 The Institution shall provide to NASFAA sufficient data for NASFAA to conduct a preliminary review of the Institution’s financial aid delivery process. This data shall be provided by the Institution not later than two (2) weeks prior to the peer review. The data provided shall include, but not be limited to the following: i) the Institution’s demographic data including, but not limited to enrollment data, Institutional type and control, annual reports, financial data, organizational charts, Institutional calendars, department calendars, web page addresses; ii) copies of federal compliance audits or reviews conducted within the last five (5) years; iii) fiscal operation reports; iv) the Institution’s sampling capabilities; v) summary of hardware/software used by the Institution’s financial aid and bursar’s office;
Obligations of Institution. Institution is responsible to Pfizer for compliance by all personnel who participate in the conduct of the Study, including the Principal Investigator and any contractors or consultants, with the terms of this Agreement and the applicable Study Order.
