ГОСТ 33647—2015
metadata3.6.6
micro-arrays3.3.33
migration of data3.6.7
multy-site study3.3.15
non-clinical health and environmental safety study3.3.1
peripheral components3.5.3
primary cells3.3.23
principal investigator3.2.7
principles of good laboratory practice (GLP)3.1.1
proprietary material3.3.24
quality assurance programme3.3.6
raw data3.3.12
recognised technical standards3.5.4
reference item, «control item»3.3.19
regulatory authority3.1.2
short-term study3.3.13
software — application3.5.5
software — operating system3.5.6
source code3.5.7
specimen3.3.18
sponsor3.2.5
standard operating procedures; SOPs3.3.7
study audit3.4.5
study initiation date3.3.10
study completion date3.3.11
study director3.2.6
study initiation date3.3.10
study plan3.3.2
study plan amendment3.3.3
study plan deviation3.3.4
system owner3.6.8
test facility3.2.1
test facility inspection3.4.4
test facility management3.2.3
test item3.3.17
test kit3.3.37
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