The Institution and Investigator agree. To conduct the Study and to accept responsibility for conduct of the Study by members of Study Team, under Investigator’s supervision, in strict accordance to the final, signed Protocol, as it may be amended, and this Agreement. The Institution and Investigator warrant that they have obtained and shall maintain all valid permits, authorisations and approvals necessary to perform their activities under the Study. The Institution and Investigator also warrant, they shall use their best efforts in performing their activities within the Study (resolve all data queries from Pharm-Olam or Sponsor within 5 days), cooperate with Pharm-Olam and Sponsor in their duties to monitor the Study and further ensure strict compliance with:
Appears in 4 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
