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They also could devise their own tests, or use tests developed by a third party, provided that the tests were approved by the state.
All procedures and tests were approved by the Institutional Animal Care Committee and adhered to the guidelines of the US Institute of Laboratory Animal Research's Guide for the Care and Use of Laboratory Animals.
All procedures and tests were approved by the Institutional Animal Care Committee of Peking Union Medical College.
The sensory evaluation tests were approved by the Jiang Nan University Institutional Review Board IRBB) and were conducted in a state-of-the-art sensory laboratory.
Cervista HPV HR and COBAS 4800 HPV tests were approved by the FDA in 2009 and 2011, respectively, for the triage of women older than the age of 21 years with diagnosis of ASCUS and for determining the presence of carcinogenic HPV types in conjunction with cytology in women older than 30 years.
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The wording of the tests was approved by the Standards and Testing Agency, an executive agency of the Department for Education.
Drugmakers play high-stakes roulette in clinical trials; only one in five drugs that enter human tests is approved.
Currently three tests are approved for the estimation of neutralizing antibodies after rabies vaccination: the mouse neutralization test (MNT), the rapid fluorescent focus inhibition test (RFFIT), and the fluorescent antibody virus neutralization (FAVN) test.
Usage of human sera for virus neutralization tests was approved by the ethical committee of the HHU Düsseldorf, Germany (#3414/2010).
The diagnosis of both groups and blood tests was approved by gastroenterologist.
The indication of breath tests was approved by experienced board-certified pediatric gastroenterologists at the Dept. of Pediatric Gastroenterology of the University Children's Hospital Münster (Germany).
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