Deviations from Protocol. Provider shall not, and shall cause Principal Investigator not to, deviate from the Protocol, except as necessary to eliminate immediate hazards to the safety and welfare of an individual participating in the Study (each, a “Subject”) and in conformity with the generally accepted standards of the medical community.
Deviations from Protocol. Site shall not, and shall cause PI not to, deviate from the Protocol, except as necessary to eliminate immediate hazards to the safety and welfare of an individual participating in the Study (each, a “Subject”) and in conformity with the generally accepted standards of the medical community. (e) Third Party Designees. Sponsor may retain one or more third parties to assist Sponsor in managing the Study. Site acknowledges Sponsor’s right to assign or transfer, in whole or in part, without the consent of Site, any of its rights or obligations under this Agreement to any such third party. Site shall permit such third party to perform any or all of Sponsor’s obligations, or to exercise any or all of Sponsor’s rights, under this Agreement. (f)
Deviations from Protocol. Except in the case of a medical emergency or otherwise as necessary for Subject safety, neither the Institution, the Principal Investigator nor Subinvestigator will make any changes in, nor deviate from, the Protocol without the Company’s prior written approval and in coordination with the supervising IRB.
