FDA Documents of Concordia Clinical Research (IRB)
Concordia Clinical Research (IRB) is an organization that has been audited by the FDA 4 times between 2000 and 2010 across all 1 sites.
Documents
FDA 483 Concordia Clinical Research (IRB), Cedar Knolls | 2010
Out-of-stock
Issued on: Dec 30, 2010
Human Drug Form 483
FDA 483 Concordia Clinical Research (IRB), Cedar Knolls | 2004
Out-of-stock
Issued on: Aug 30, 2004
Human Drug Form 483
FDA 483 Concordia Clinical Research (IRB), Cedar Knolls | 2003
Out-of-stock
Issued on: Jun 24, 2003
Human Drug Form 483
FDA 483 Concordia Clinical Research (IRB), Cedar Knolls | 2000
Out-of-stock
Issued on: Aug 2, 2000
Human Drug Form 483