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CyberTRIZPEDIA
/ Research
Research
18 regulations apply to this sector.
Written for this sector
21 CFR 50/56
Applies to clinical researchers conducting FDA-regulated human subjects research
21 CFR 58
Applies to laboratories conducting nonclinical safety studies for FDA submissions
21 CFR 812
Governs researchers and sponsors conducting clinical investigations of medical devices
ISO 22989
Research institutions use the standard to align AI terminology in publications.
ISO 23053
Research organisations use the framework for structured ML development methodology.
Also applies
AI EO
EO promotes AI research investment and safety research initiatives
CHIPS
CHIPS Act funds semiconductor R&D programs at research institutions
DGA
Data altruism and research data sharing mechanisms established by DGA.
FDA 21 CFR 812
Research institutions conducting clinical device investigations must comply with IDE rules
GIIN IRIS Plus
Researchers and evaluators use IRIS+ taxonomy for standardised impact measurement.
GIIN-IRIS
IRIS taxonomy used by researchers for standardised social impact measurement.
IAEA Statute
Nuclear research reactors and scientific facilities fall under IAEA safeguards.
ISO 14155
Clinical research organisations conducting device trials must follow ISO 14155
ISO 23894
Research bodies apply AI risk guidance to responsible AI development projects.
ISO 56002
Research organisations adopt innovation management frameworks from ISO 56002
IVDR
Research labs developing diagnostic tests must consider IVDR applicability.
NIST AI RMF
Research institutions developing AI systems apply this framework.
Regulation (EU) 2021/697 European Defence Fund
EDF supports defence-related research and innovation activities.