Common use of Obligations of Institution and Principal Investigator Clause in Contracts

Obligations of Institution and Principal Investigator. Institution and Principal Investigator 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 and Principal Investigator 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 1.

Obligations of Institution and Principal Investigator. Institution and Principal Investigator will ensure that Research Staff is 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 and Principal Investigator will assume all those responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards including, including without limitation, 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 1.”

Obligations of Institution and Principal Investigator. Institution and Principal Investigator 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 and Principal Investigator will assume all those responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards applicable in the Czech Republic 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 1.

Obligations of Institution and Principal Investigator. Institution and Principal Investigator 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 and Principal Investigator will assume all those responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards laws and/or regulations 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 1.

Obligations of Institution and Principal Investigator. Institution and Principal Investigator 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 and Principal Investigator will assume all those responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards including, without limitation, all relevant International Conference on Council for Harmonization Good Clinical Practice (“ICH GCP”) guidelines and standards and the World Medical Association declaration 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 1.Human

Obligations of Institution and Principal Investigator. Institution and Principal Investigator 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 and Principal Investigator will assume all those responsibilities assigned under all applicable laws, rules, regulations, guidelines and standards in force in the Czech Republic 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 1.