A protocol for animal studies was approved by Institutional animal ethical committee and project number was 03.
Already, Health Canada has approved a protocol for a human trial with interferon alone, without steroids or ribavirin, in case SARS reemerges.
In 2011, the FDA approved a protocol for her proposed study investigating the effects of whole-plant marijuana on veterans suffering from PTSD.
The Ohio Department of Health and Human Subjects Institutional Review Board approved a protocol for this study.
In Robertson v. McGee [ 4], the REC had approved a protocol for a Phase I study of a cancer vaccine.
A protocol for archival tissue collection was approved by Institutional Review Board at both institutions with a waiver of consent.
A protocol for the study was reviewed and approved by two independent committees, one with experts from South Asia, the other with experts in conducting literature reviews.
A protocol was approved for all animal use in this study by the FDA White Oak Institutional Animal Care and Use Committee.
The orthotopic tumor model for glioblastoma on a protocol was approved by the Shanghai Jiao-Tong University Animal Care and Use Committee.
Four- to 5-week-old NOD/SCID mice (Charles River Laboratories) were housed in a facility certified by the Canadian Council of Animal Care and used for this study according to a protocol approved by The Hospital for Sick Children Animal Care Committee.
All experiments were carried out in BALB/c mice according to a protocol approved by the Committee for Animal Experiments for the Canton Vaud, Switzerland (permits 2316 and 2464).
