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.
2. Institution will provide WGU with timely curricular updates of all updates of all offered degrees, certificates, and educational programs.
3. Institution will establish a web link from its internal websites to the WGU articulation pathways page (xxxxxxxx.xxx.xxx).
4. If Institution offers other tuition assistance programs, WGU programs will be added to the list of programs eligible for Institution’s highest level of assistance.
5. Institution will invite WGU to participate in any education/benefit fairs, information seminars, and “lunch and learn” presentations that Institution may offer.
6. Institution agrees to support additional marketing communications upon request.
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”).
Obligations of Institution. Institution will ensure that any personnel who assist in the conduct of the Trial are 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 related to the confidentiality, privacy and security of Trial Subjects information, inclusive but not limited to the EU General Data Protection Regulation –GDPR- (“Applicable Law”). zdravotnického zařízení, bude xxxxxx (dále jen “hlavní zkoušející”) se sídlem U Nemocnice 499/2, 128 08 Xxxxx 0, Xxxxx xxxxxxxxx, který bude odpovědný za vedení klinického hodnocení v souladu s platnými předpisy zdravotnického zařízení. Klinické hodnocení bude prováděno pod vedením hlavního zkoušejícího ve Všeobecné fakultní nemocnici v Praze, xxxx, U Nemocnice 499/2, 128 08 Xxxxx 0, Xxxxx xxxxxxxxx. Zdravotnické zařízení souhlasí, aby společnost INC Research uzavřela s hlavním zkoušejícím a/nebo případně s dalšími výzkumnými pracovníky samostatnou smlouvu o klinickém hodnocení, na základě které, se hlavní zkoušející zaváže, že on i jeho výzkumný personál provedou klinické hodnocení a že tato samostatná smlouva bude obsahovat spravedlivou odměnu.
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").
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.
Obligations of Institution. Institution will ensure that any personnel who assist in the conduct of the Trial are 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” (1996), all applicable laws and guidance
Obligations of Institution. Institution is responsible to Sponsor and 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 abide by all terms of this Agreement applicable to the activities they perform. In the extent required by the applicable legislation, the Institution will assume all those responsibilities for due performance of the Trial at the Trial Site assigned under all applicable laws, legal rules, regulations, guidelines and standards, including without limitation, all relevant International Conference on Harmonization Good Clinical Practice (“ICH GCP”) guidelines and standards, and all applicable laws relating to the confidentiality, privacy and security of patient information ("Applicable Law").
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,
b) The Institution guarantees that the appropriate facilities at the Site, including any equipment, but excluding that to be provided by získaných během Studie („Studijní data“) za účelem vyplnění formulářů pro záznamy subjektů hodnocení („CRF“) v souladu s Protokolem a učinění příslušných opatření k zajištění jejich správnosti a úplnosti, dále bezodkladná kompletace a předání CRO těchto kompletních CRF, f) informování Xxxxxxxxxx, CRO, Etické komise a Multicentrické etické komise o jakémkoli odchýlení se od Protokolu a správné klinické praxe nebo jejich nedodržování v souladu s touto Smlouvou,
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 acknowledges and agrees for compliance by all employees of the Institution with the terms of this Agreement. Institution acknowledges and agrees that any Institution employee who assist in the conduct of the Trial are informed of and agree to abide by all terms of this Agreement applicable to the activities they perform. Institution acknowledges all those responsibilities assigned to Institution 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 all applicable laws relating to the confidentiality, privacy and security of patient information ("Applicable Law").
