8. Manufacturers do not require to implement any cybersecurity program for the software used as a medical device or software part of any medical device d ne nawtoe oteoimummoo A. True В. False 9. Design validation must be completed prior to design verification. A. seleS True В. False OS8 ARO of pnibtoooAS nem 10. The firm must have a written quality plan that defines the quality practices, resources, and activities relevant to the devices that are being designed and manufactured at that facility. 5 bris bo boon Jon ob eir oob sisloedC А. True В. False

Computer Networking: A Top-Down Approach (7th Edition)
7th Edition
ISBN:9780133594140
Author:James Kurose, Keith Ross
Publisher:James Kurose, Keith Ross
Chapter1: Computer Networks And The Internet
Section: Chapter Questions
Problem R1RQ: What is the difference between a host and an end system? List several different types of end...
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Question
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8. Manufacturers do not require to implement any cybersecurity program for the software
used as a medical device or software part of any medical device
A.
True
o beeaiieo
B.
SUOL COLJnu
False
9. Design validation must be completed prior to design verification.
A.
sels
True
В.
False
10. The firm must have a written quality plan that defines the quality practices, resources,
and activities relevant to the devices that are being designed and manufactured at that
facility.
of boon Jon ob ein
eloedoE
A.
True
В.
False
sels
nengbleveb eoivab leolbem dose nol meteye vilsuo s agoleveb A A
Output
User needs and Design Inpu
LA
clude
eale
nemmoo tot sieb yd behogque ed of beon Jon ob soiveb Isoibem yne not amislo.
Device
and
SUT
eels
B:
ACR o lavoce oubog nodenidmoo ooiveb-gunb s 10R.0
lleao a punb er puno lue ne lo bealani odeosla
pniteel
elo
hoogue atab huoni
no Jon ban lioca s
ole
Page 6 of 16
Transcribed Image Text:8. Manufacturers do not require to implement any cybersecurity program for the software used as a medical device or software part of any medical device A. True o beeaiieo B. SUOL COLJnu False 9. Design validation must be completed prior to design verification. A. sels True В. False 10. The firm must have a written quality plan that defines the quality practices, resources, and activities relevant to the devices that are being designed and manufactured at that facility. of boon Jon ob ein eloedoE A. True В. False sels nengbleveb eoivab leolbem dose nol meteye vilsuo s agoleveb A A Output User needs and Design Inpu LA clude eale nemmoo tot sieb yd behogque ed of beon Jon ob soiveb Isoibem yne not amislo. Device and SUT eels B: ACR o lavoce oubog nodenidmoo ooiveb-gunb s 10R.0 lleao a punb er puno lue ne lo bealani odeosla pniteel elo hoogue atab huoni no Jon ban lioca s ole Page 6 of 16
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