Montreal, QC – August 8, 2017 – Veritas IRB is proud to announce that it has been approved by the Ministry of Health in Saskatchewan to perform research ethics review in the province. According to the Ministry of Health’s order No. 2017-06 of May 2, 2017, Veritas IRB has specifically been approved as a Research […]
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Central IRB, Clinical Trials, Research Participants, Uncategorised
IntegReview IRB and Veritas IRB announce partnership to provide accredited ethics review services in the U.S. and Canada
16
May
May
Austin, Texas and Montreal, Canada – IntegReview IRB partnered with Canadian-based Veritas IRB Inc., to provide ethics review services and risk management consulting to sponsors of research and investigators in both the United States and Canada. Veritas IRB was the first Canadian organization ever to be accredited by the Association for […]
10
Nov
Nov
Based on Canadian and American regulations, research sponsors must obtain the right to distribute and use an investigational drug for the purpose of a clinical trial. In both countries, sponsors of research must file an application to the applicable regulatory agency. This will exempt sponsors from the traditional approval requirements that are necessary to import […]