Common use of Role as Principal Investigator Clause in Contracts

Role as Principal Investigator. Investigator shall serve as the principal investigator for the Study at Institution, and shall personally conduct and/or supervise all aspects of the Study, including reviewing, signing, and dating Idorsia supplied case report forms which record all of the Protocol-required information to be reported to Idorsia for each Subject (defined below) ("CRFs"). Prior to commencing the Study, Investigator shall have read and understood the information contained in the Investigator's brochure. Institution or Investigator shall submit the following to Idorsia before conducting the Study and shall retain copies for Regulatory Authority review: (i) Investigator's current curriculum vitae, (ii) documentation of all IRB/IEC approvals in accordance with Section 1.2.1 (IRB/IEC review), and (iii) a copy of the IRB/IEC- approved ICF (as defined below) to be used in the Study. Investigator shall use his/her best efforts to recruit Study Subjects (as defined below), who are in Investigator's reasonable judgment, likely to be eligible and sufficiently reliable to complete the entire Study.

Role as Principal Investigator. Investigator shall serve as the principal investigator for the Study at Institution, and shall personally conduct and/or supervise all aspects of the Study, including reviewing, signing, and dating Idorsia supplied case report forms which record all of the Protocol-required information to be reported to Idorsia for each Subject (defined below) ("CRFs"). Prior to commencing the Study, Investigator shall have read and understood the information contained in the Investigator's brochure. Institution or Investigator shall submit the following to Idorsia before conducting the Study and shall retain copies for Regulatory Authority review: (i) Investigator's current curriculum vitae, (ii) documentation of all IRB/IEC approvals in accordance with Section 1.2.1 (IRB/IEC review), and (iii) a copy of the IRB/IEC- IEC-approved ICF (as defined below) to be used in the Study. Investigator shall use his/her best efforts to recruit Study Subjects (as defined below), who are in Investigator's reasonable judgment, likely to be eligible and sufficiently reliable to complete the entire Study.

Role as Principal Investigator. Investigator shall serve as the principal investigator for the Study at Institution, and shall personally conduct and/or supervise all aspects of the Study, including reviewing, signing, and dating Idorsia supplied case report forms which record all of the Protocol-required information to be reported to Idorsia for each Subject (defined below) ("CRFs"). Prior to commencing the Study, Investigator shall have read and understood the information contained in the Investigator's brochure. Institution or Investigator shall submit the following to Idorsia before conducting the Study and shall retain copies for Regulatory Authority review: (i) Investigator's current curriculum vitae, (ii) documentation of all IRB/IEC approvals in accordance with Section 1.2.1 (IRB/IEC review), and (iii) a copy of the IRB/IEC- approved ICF (as defined below) to be used in the Study. Investigator shall use his/her best efforts to recruit Study Subjects (as defined below), who are in Investigator's reasonable judgment, likely to be eligible and sufficiently reliable to complete the entire Study.

Role as Principal Investigator. Investigator shall serve as the principal investigator for the Study at Institution, and shall personally conduct and/or supervise all aspects of the Study, including reviewing, signing, and dating Idorsia Actelion supplied case report forms which record all of the Protocol-Protocol- required information to be reported to Idorsia Actelion for each Subject (defined below) ("CRFs"). Prior to commencing the Study, Investigator shall have read and understood the information contained in the Investigatorinvestigator's brochure. Institution or Investigator shall submit the following to Idorsia Actelion before conducting the Study and shall retain copies for Regulatory Authority review: (i) Investigator's current curriculum vitae, (ii) documentation of all IRB/IEC approvals in accordance with Section 1.2.1 (IRB/IEC review), and (iii) a copy of the IRB/IEC- approved ICF (as defined below) to be used in the Study. Investigator shall use his/her best efforts to recruit Study Subjects (as defined below), who are in Investigator's reasonable judgment, likely to be eligible and sufficiently reliable to complete the entire Study.