Related articles:
Pharmacovigilance
Institutional review board
Informed consent
Placebo
Randomized controlled trial
National Institutes of Health
Case-control study
Evidence-based medicine
In vitro
Effectiveness
Interactive voice response
Avicenna
Rofecoxib
In vivo
Epidemiology
Cohort study
Blind experiment
Health care
Key terms:
clinical trials
irb
sponsor
investigators
ich
phase iii
cro
randomized
phase iv
informed consent
adverse event
local investigator
pharmacokinetic
regulatory agency
harmonization
phase i trials
phase ii trials
phase iii trials
healthy volunteers
local irb
medication or device
appropriate regulatory
multicenter
local site investigators
observational studies
good clinical practice
regulatory authorities
randomized controlled trial
pharmaceuticals for human use
pharmacodynamics
assess the safety and effectiveness
potential benefits
technical requirements for registration
legally authorized
registration of pharmaceuticals for human
ethical conduct
ethics committee
clinical trial protocol
conference on harmonization of technical
adverse event reports
pharmaceutical companies
national institutes of health
requirements for registration of pharmaceuticals
ich guidelines
sponsor is responsible
international conference on harmonization
local investigators are responsible
sponsoring company
many clinical trials
harmonization of technical requirements
Search external links cited by footnotes on Wikipedia page Clinical trial:
|
|