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The last approvals date back to January.
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IMB Application date 12.03.07 Approval date 27.04.07 Clinical trials approved committee Approval date 29.11.07 Data will be collected in duplicate on a case report form (CRF) at the time of recruitment by a trained researcher.
Cancer studies (Family-Cancer Database) in the MigMed Database was approved by the Lund regional ethical committee on 8/12/2008 (No. 409/2008) and with complementary approvals dated 9/1/2009 and 1/22/2010.
A second 6 month extension, for a total of 18 months from the original approval date, may be approved by the FSA State Committee.
Recruitment of study participants was performed according to protocol (ClinicalTrials.gov ID NCT01489839) approved by Forsyth Institutional Review Board ID #11-09 (Approval Date 8 August 2014) in Cambridge, MA, USA.
All studies were performed in accordance with the Guide for the Care and Use of Laboratory Animals, and all procedures were approved by The Jackson Laboratory Animal Care and Use Committee, comprehensive protocol #01026, approval date Nov. 29, 2007.
The whole blood sample for this study was collected under a protocol approved by the University of Louisville IRB (IRB tracking number 11.0659, approval date 1/30/2012).
Our findings of regional variation are unlikely the result of differential reimbursement for bevacizumab since the US Centers for Medicare & Medicaid Services CMSS) approved coverage for bevacizumab retroactive to the FDA approval date.
Administration of the survey was approved by the Human Research Protection Office of Washington University in St . Louis(IRB ID 201104105; approval date 12 April 2012).
The study was approved by the local Scientific and Ethical Committee (approval number MGRL001 approval date 6/4/2008).
The use of CT was approved by the local ethics review committee (REC reference 07/Q0401/25, approval date August 13 , 2007.
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