Common use of Conduct of Study Clause in Contracts

Conduct of Study. The Site shall, and shall ensure that its employees and agents shall, conduct the Study in strict compliance with any and all applicable federal, national, state, local or other jurisdictional laws, rules, regulations, policies, guidelines, guidances, and governmental requirements, as may be applicable to the Parties, Study Personnel, and/or the Study (“Applicable Law”), including without limitation: i. all applicable rules, policies, or guidance issued by the European Medicines Agency (“EMA”); ii. the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (“ICH”) Guidelines for Good Clinical Practices as adopted or issued by any governmental or other regulatory authority, including FDA and EMA (collectively, “GCP” or “GCP Guidelines”), iii. all applicable laws and regulations regarding the protection of privacy, personal data, and medical data, including the European Data Protection Directive (95/46/EC) (collectively, the “Privacy Regulations”); iv. all applicable state HIV testing laws; v. all applicable local,

Conduct of Study. The Site shall, and shall ensure that its employees and agents shall, conduct the Study in strict compliance with any and all applicable federal, national, state, local or other jurisdictional laws, rules, regulations, policies, guidelines, guidances, and governmental requirements, as may be applicable to the Parties, Study Personnel, and/or the Study (“Applicable Law”), including without limitation: i. all applicable rules, policies, or guidance issued by the European Medicines Agency (“EMA”); ii. the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (“ICH”) Guidelines for Good Clinical Practices as adopted or issued by any governmental or other regulatory authority, including FDA and EMA (collectively, “GCP” or “GCP Guidelines”), iii. all applicable laws and regulations regarding the protection of privacy, personal data, and medical data, including the European Data Protection Directive (95/46/EC) (collectively, the “Privacy Regulations”); iv. all applicable state HIV testing laws; v. all applicable local,předpisy týkající se testování HIV;

Conduct of Study. The Site shall, and shall ensure that its employees and agents shall, conduct the Study in strict compliance with any and all applicable federal, national, state, local or other jurisdictional laws, rules, regulations, policies, guidelines, guidances, and governmental requirements, as may be applicable to the Parties, Study Personnel, and/or the Study (“Applicable Law”), including without limitation: i. all applicable rules, policies, or guidance issued by the European Medicines Agency (“EMA”); ii. the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (“ICH”) Guidelines for Good Clinical Practices as adopted or issued by any governmental or other regulatory authority, including FDA and EMA (collectively, “GCP” or “GCP Guidelines”), iii. all applicable laws and regulations regarding the protection of privacy, personal data, and medical data, including the European Data Protection Directive (95/46/EC) (collectively, the “Privacy Regulations”); iv. all applicable state HIV testing laws; v. all applicable local,, state, federal, and national laws and a právní předpisy týkající se hlášení všech poplatků a jiných výdajů placených zdravotníkům