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These template forms are issued by HSA solely for the purpose of facilitating the conduct of your clinical trial.
A separate form for each clinical trial site must be completed by the Sponsor and filed with Health Canada.
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Clinical trial endpoints. u Ian Tannock has reported no conflict of interest relevant to this presentation u Steinar Aamdal has reported no conflict of interest u Dirk Arnold has reported to have received honoraria for educational activities/Advisory role from..clinical study report writing which include Clinical sections of IND, INDAs, ANDA, NDS, ANDS, Protocol writing, Labeling justification, Pre-submission package, IND application documents & meeting support and supports Abbreviated ICF, PASS studies (Post Authorization Safety studies) report. What were the important questions asked in the trial? Clinical Study Reports (CSRs) are often created as part of the process of submitting applications for new medical treatments to regulators.
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