Season 6: Episode 1
What to Learn in this Video ?
1) What is a medical device.
2) What is Product Development Life Cycle.
3) US FDA Medical Device Classifications and Examples.
4) EU MDR Medical Device Classifications and Examples.
5) DO 178C Software Levels ABCDE.
Credits and Links for further Study:
/ @gptechstoriesinkannada
https://www.pacificbridgemedical.com/...)
https://cdsco.gov.in/opencms/opencms/...
https://www.fda.gov/medical-devices/p...
https://www.news-medical.net/health/M....
https://www.fda.gov/medical-devices/o...
https://www.greenlight.guru/glossary/....
https://www.qualio.com/resources/medi...
https://www.fda.gov/medical-devices
https://www.greenlight.guru/blog/ques...
https://www.greenlight.guru/blog/ce-m...
https://en.wikipedia.org/wiki/DO-178C
https://www.google.com/search?q=what+...
Tags:
#usfda
#EUMDR
#medicaldevices
#DesignControls
#MedicalDeviceClassifications
#MedicalDeviceExamples
#BasicsOfMedicalDeviceClassification
#kannadalearning
#tutorialsinkannada
#PDLMinKannada
#productlifecycle
#howtoclassifymedicaldeviceinkannada
fda medical device classification, medical device classification eu, medical device classification, medical device classification panel fda, fda medical device classifications, medical devices classification eu, fda classification of medical devices, medical devices classification, medical devices classification usa, medical device software classification, medical device classifications, fda device classification, device classification, fda medical device classes, fda medical device regulations, software, software testing, do178c, d0178c, do-178c, do178, do178b, medical device regulation europe, mdr europe medical device regulation, medical device development, medical device adverse event reporting in eu, new to medical device sales, medical device reporting requirements in us, regulation in medical devices, medical device academy, medical device products, medical device manufacturers, medical device, medical device sales, medical device training, medical devices, learn medical devices, eu medical device regulation, medical device adverse event reporting requirements
Информация по комментариям в разработке