Compliance with Laws, Regulations, and Good Clinical Practices. Site agrees that Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol), any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs, Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some
Compliance with Laws, Regulations, and Good Clinical Practices. Site agrees that Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol (enclosed hereto as Attachment B), any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs, Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some related acts (“Act on Pharmaceuticals”) and Decree No. 226/2008 Coll., on good clinical practice and detailed conditions of clinical trials on medicinal products, as amended, Act No. 372/2011 Coll., on Medical Services and terms and conditions of performance of
Compliance with Laws, Regulations, and Good Clinical Practices. Institution agrees that Investigator shall conduct the Study in accordance with the terms of this Agreement and applicable laws and regulations and Institution agrees that the Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol, any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs and applicable laws related to data protection and data privacy, including without limitation, the Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC (General Data Protection Regulation - “GDPR”), Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some related acts (“Act on Pharmaceuticals”) and Decree No. 226/2008 Coll., on good clinical practice and
Compliance with Laws, Regulations, and Good Clinical Practices. Site agrees that Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol (as amended), the written instructions from Sponsor and/or IQVIA, applicable direction received from the institutional review board/ Ethic Committee (where applicable), any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs, Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some related acts (“Act on Pharmaceuticals”) and Decree No. 226/2008 Coll., on good clinical practice and detailed conditions of clinical trials on medicinal products, as amended, Act No. 372/2011 Coll., on Medical Services and terms and conditions of performance of such services („Act on Medical Services“) or any subsequent amendments or laws substantially replacing any of the foregoing.(together “Applicable Laws”). Site and Study Staff acknowledge that IQVIA and Sponsor, and their respective affiliates, need to adhere to the provisions of (i) the Bribery Act 2010 of the United Kingdom (Bribery Act); (ii) the Foreign Corrupt Practices Act 1977 of the United States of America (FCPA), (iii) the French Anticorruption Law named “Sapin II Law” (2016) and (iii) any other applicable anti-corruption legislation. Sponsor and IQVIA hereby undertake not to conclude any other contract in connection with this Study with any employee of the Institution.
Compliance with Laws, Regulations, and Good Clinical Practices. 1.1 Soulad s Právními předpisy, nařízeními a Správnou klinickou praxí Site agrees that Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol, any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs, Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some related acts (“Act on Pharmaceuticals”) and Decree No. 226/2008 Coll., on good clinical practice and detailed conditions of clinical trials on medicinal products, as amended, Act No. 372/2011 Coll., on Medical Services and terms and conditions of performance of such services („Act on Medical Services“) or any subsequent amendments or laws substantially replacing any of the foregoing.(together “Applicable Laws”). Site and Study Staff acknowledge that Quintiles and Sponsor, and their respective affiliates, need to adhere to the provisions of (i) the Xxxxxxx Xxx 0000 of the United Kingdom (Bribery Act); (ii) the Foreign Corrupt Practices Xxx 0000 of the United States of America (FCPA) and (iii) any other applicable anti-corruption legislation. Místo provádění klinického hodnocení souhlasí s tím, že Místo provádění klinického hodnocení a Studijní personál provede ve Zdravotnickém zařízení Studii v přísném souladu s touto Smlouvou, Protokolem, veškerými příslušnými právními předpisy a nařízeními, zejména včetně GCP, zák. č. 378/2007 Sb., o léčivech a změnách některých souvisejících zákonů (“Zákon o léčivech”) a Vyhlášky č. 226/2008 Sb., o správné klinické praxi a bližších podmínkách klinického hodnocení léčivých přípravků, v platném znění, zák. č. 372/2011 Sb., o Zdravotních službách a podmínkách jejich poskytování („Zákon o zdravotních službách“) nebo jakýchkoli následných pozměňujících či podstatně nahrazujících právních předpisů ve vztahu ke shora uvedeným právním normám, (společně “Příslušné právní předpisy”). Místo provádění klinického hodnocení a Studijní personál tímto berou na vědomí, že Quintiles a Zadavatel, a jejich odpovědné pobočky, se zavazují dodržovat (i) britský zákon proti korupci z roku 2010 (“Protikorupční zákon”); (ii) zákon USA z roku 1977 o zahraničních korupčních praktikách z roku 1977 (“FCPA”) a (iii) jakékoli další právní přepisy na úseku zákazu korupčních praktik.
Compliance with Laws, Regulations, and Good Clinical Practices. Site agrees that Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol, any and all applicable local, national and international laws regulations and guidelines, including in particular, but without limitation, GCPs. Site and Study Staff acknowledge that Quintiles and Sponsor, and their respective affiliates, need to adhere to the provisions of (i) the Bribery Act 2010 of the United Kingdom (Bribery Act); (ii) the Foreign Corrupt Practices Act 1977 of the United States of America (FCPA) and (iii) any other applicable anti- corruption legislation.
Compliance with Laws, Regulations, and Good Clinical Practices. 1.1 Soulad s Právními předpisy, nařízeními a Správnou klinickou praxí Site agrees that Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol, any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs, Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some related acts (“Act on Pharmaceuticals”) and Decree No. 226/2008 Coll., on good clinical practice and detailed conditions of clinical trials on medicinal products, as amended, Act No. 372/2011 Coll., on Medical Services and terms and conditions of performance of such services („Act on Medical Services“) or any subsequent amendments or laws substantially replacing any of the foregoing.(together “Applicable Laws”). Site and Study Staff acknowledge that Quintiles and Sponsor, and their respective affiliates, need to adhere to the provisions of (i) the Xxxxxxx Xxx 0000 of the United Kingdom (Bribery Act); (ii) the Foreign Corrupt Practices Xxx 0000 of the United States of America (FCPA) and (iii) any other applicable anti-corruption legislation. Site acknowledges to have, at all times during the course of the Study, appropriate licenses, approvals and certifications necessary to safely, adequately and lawfully perform the Study in accordance with GCPs, regulatory requirements and all applicable laws, and has no notice of any investigations that would jeopardize such licenses, approvals or certifications. This section 1.1 shall survive termination or expiration of this Agreement. Místo provádění klinického hodnocení souhlasí s xxx, že Místo provádění klinického hodnocení a Studijní personál provede ve Zdravotnickém zařízení Studii v přísném souladu s touto Smlouvou, Protokolem, veškerými příslušnými právními předpisy a nařízeními, zejména včetně GCP, zák. č. 378/2007 Sb., o léčivech a změnách některých souvisejících zákonů (“Zákon o léčivech”) a Vyhlášky č. 226/2008 Sb., o správné klinické praxi a bližších podmínkách klinického hodnocení léčivých přípravků, v platném znění, zák. č. 372/2011 Sb., o Zdravotních službách a podmínkách jejich poskytování („Zákon o zdravotních službách“) nebo jakýchkoli následných pozměňujících či podstatně nahrazujících právních předpisů ve vztahu ke shora uvedeným právním normám, (společně “Příslušné právní předpisy”). Místo provádění klinického hodnocení a Studijní personál tímto berou na vědomí, že Quintiles a Zadavatel, a jejich odpovědné pobočky, se zav...
Compliance with Laws, Regulations, and Good Clinical Practices. Site agrees that Site and Study Staff shall perform the Study at Provider in strict accordance with this Agreement, the Protocol (enclosed hereto as Attachment B), any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs, Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some related acts (“Act on Pharmaceuticals”) and Decree No. 226/2008 Coll., on good clinical practice and detailed conditions of clinical trials on medicinal products, as amended, Act No. 372/2011 Coll., on Medical Services and terms and conditions of performance of such services („Act on Medical Services“) or any subsequent amendments or laws substantially replacing any of the foregoing.(together “Applicable Laws”). Site and Study Staff acknowledge that Quintiles and Sponsor, and their respective affiliates, need to adhere to the provisions of (i) the Xxxxxxx Xxx 0000 of the United Kingdom (Bribery Act); (ii) the Foreign Corrupt Practices Xxx 0000 of the United States of America (FCPA) and (iii) any other applicable anti-corruption legislation.
Compliance with Laws, Regulations, and Good Clinical Practices. Site agrees that Site and Study Staff shall perform the Study at Institution in strict accordance with this Agreement, the Protocol, any and all applicable laws regulations and guidelines, including in particular, but without limitation, GCPs, Act No. 378/2007 Coll., on Pharmaceuticals and on amendments to some related acts (“Act on Pharmaceuticals”) and Decree No. 226/2008 Coll., on good clinical practice and detailed conditions of clinical trials on medicinal products, as amended, Act No. 372/2011 Coll., on Medical Services and terms and conditions of performance of such services („Act on Medical Services“) or any subsequent amendments or laws substantially replacing any of the foregoing (together “Applicable Laws”). Site and Study Staff acknowledge that IQVIA and Sponsor, and their respective affiliates, need to adhere to the provisions of (i) the Bribery Act 2010 of the United Kingdom (Bribery Act); (ii) the Foreign Corrupt Practices Act 1977 of the United States of America (FCPA) and (iii) any other applicable anti-corruption legislation.
Compliance with Laws, Regulations, and Good Clinical Practices. Institution agrees that Institution, its Investigator and Study Staff shall perform the Study, exercising due care at Institution in accordance with this Agreement, the Protocol, Applicable Laws, and GCPs. XXXXX agrees that it and Sponsor, and their respective Affiliates, shall adhere to all (i) Applicable Laws (ii) the Bribery Act 2010 of the United Kingdom (Bribery Act); (ii) the Foreign Corrupt Practices Act 1977 of the United States of America (FCPA) and (iii) any other applicable anti-corruption legislation.
