作者: LESLEY SEYMOUR , SENIOR BIOSTATISTICIAN , DONGSHENG TU
DOI:
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摘要: I have read the protocol and agree that it contains all necessary details for carrying out the study as described. I will conduct this protocol as outlined therein, and according to Good Clinical Practice and any applicable local regulations. I will make a reasonable effort to complete the study within the time designated. I confirm that I and study personnel participating under my supervision have adequate resources to fulfill their responsibilities as outlined in this protocol. I will maintain documentation of any investigator responsibilities assigned to participating study personnel. I confirm that all data will be submitted in a timely manner and will be accurate, complete and supported by source documents.I will provide copies of the protocol and access to all information furnished by NCIC CTG and Oncolytics Biotech Inc. to study personnel under my supervision. I will discuss this material with them to ensure that they are fully informed about the investigational product and the study.