Personal Information
Unternehmen/Arbeitsplatz
Seattle, Washington, WA United States
Branche
Medical / Health Care / Pharmaceuticals
Webseite
www.quorumreview.com/
Info
A sustained passion for performance.
The founders of Quorum Review IRB believed that an IRB did not have to sacrifice customer service to provide a thorough review. They knew they must build a high-performance IRB. So in 1992, that’s what they set out to do. Since then, Quorum has relentlessly pursued better ways to deliver IRB services—for research participants, sponsors and CROs alike.
At Quorum, performance is in our DNA, and throughout our history, we’ve innovated to simplify and streamline for participants, sites and sponsors alike.
Quorum is the IRB of choice when performance matters, and to us it always does.
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Personal Information
Unternehmen/Arbeitsplatz
Seattle, Washington, WA United States
Branche
Medical / Health Care / Pharmaceuticals
Webseite
www.quorumreview.com/
Info
A sustained passion for performance.
The founders of Quorum Review IRB believed that an IRB did not have to sacrifice customer service to provide a thorough review. They knew they must build a high-performance IRB. So in 1992, that’s what they set out to do. Since then, Quorum has relentlessly pursued better ways to deliver IRB services—for research participants, sponsors and CROs alike.
At Quorum, performance is in our DNA, and throughout our history, we’ve innovated to simplify and streamline for participants, sites and sponsors alike.
Quorum is the IRB of choice when performance matters, and to us it always does.
Tags
irb
quorum review
quorum review irb
clinical trial
clinical research
clinical investigators
irb webinar
cami gearhart
fda guidance
ethics review
econsent
clinical studies
independent review board
canadian law
regulatory requirements
biobanking
future research
privacy
clinical trials
institutional review board
legally incapacitated adults
consent
consent form
claire carbary
irb training
social media
fda
phase 1
pharmaceutical
ebola
45 cfr 46
institutions
human subject
fwa
ohrp
health canada
appropriate documentation
medical devices
irb safety reporting
susar
unanticipated problems that are not adverse events
unanticipated problems
uade
biorepositories
hipaa
fda warning letters
electronic consent
aahrpp
jim gearhart
sunshine act
biological samples
u.s. law
webinar
ethics review board
henrietta lacks
lars
pharmaceuticals
recruitment and consent
minors
limited capacity
human research
fda guiadance
irb review
e-consent
dia
pediatric trials
study tools
irb evaluation
recruitment advertising
ide
screening subjects
history of irb
industrial supply
Mehr anzeigen