Experimental Procedures Sample Clauses
The Experimental Procedures clause defines the methods and protocols to be followed during the conduct of experiments under an agreement. It typically outlines the specific steps, materials, and conditions required for the research, ensuring that all parties adhere to a consistent and agreed-upon process. By clearly specifying how experiments should be performed, this clause helps maintain scientific integrity, reproducibility, and compliance with regulatory or safety standards.
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Experimental Procedures. The Seller Entities have not performed or permitted the performance of any experimental or research procedures or studies involving patients of any Hospital not authorized and conducted in accordance with the procedures of the Institutional Review Board of the relevant Hospital
Experimental Procedures. During the past five (5) years Seller has not performed or permitted the performance of any Experimental Procedures involving patients in the Healthcare Facilities not authorized and conducted in accordance with the procedures of the applicable Institutional Review Board.
Experimental Procedures. No Seller has performed or authorized the performance of any experimental or research procedures or studies involving patients of any Facility that require the prior approval of any governmental entity that has not been obtained.
Experimental Procedures. Sellers have not performed or permitted the performance of any experimental or research procedures or studies involving patients of the Facilities not authorized and conducted in accordance with the procedures of the Institutional Review Board of the relevant Facility.
Experimental Procedures. The Partnership has not performed or permitted the performance of any experimental or research procedures or studies involving patients of the Hospital not authorized and conducted in accordance with the procedures of the Institutional Review Board of the Hospital.
Experimental Procedures. The study protocol was approved by the University of California, Berkeley Committee for Protection of Human Subjects, following the declaration of Helsinki. All partici- pants gave written informed consent after the nature of Patient Lesion volume (cm3) % STG and MTG % AG and SMG % LIFG P1 18.32 26.9 7.4 0 P2 4.51 5.6 0 0 P3 93.75 62.3 48 0 P4 36.95 45.5 0 0 P5 103.17 22.7 21.7 21.4 P6 85.82 84.5 43.1 0 Mean (sd) 57.08 (38.68) 41.25 (28.82) 20 (21.4) 3.57 (8.74)
Experimental Procedures. The Seller Entities have not performed or permitted the performance of any experimental or research procedures or studies involving patients of the Hospital not authorized and conducted in accordance with the procedures of the Institutional Review Board of the Hospital. All human subject research (as that phrase is defined by federal Law), or research governed by the federal Animal Welfare Act, involving the Seller Entities is identified on Schedule 3.23.
Experimental Procedures. Except as previously disclosed by Seller to Buyer, since January 1, 2007, to Seller’s Knowledge, Seller has not performed or permitted the performance of any experimental or research procedures or studies involving patients in the Hospital not authorized and conducted in accordance with the procedures of an Institutional Review Board of the Hospital.
Experimental Procedures. 2.2.1. Materials
Experimental Procedures. Neither Ameris nor any Ameris Subsidiary is performing or permitting the performance of any experimental or research procedures or studies involving parties in Smit▇ ▇▇▇pital, Hermitage Hall, the Clarksville Home, the Alabama Program or the Philadelphia Program or otherwise.