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Clinical Investigators - Disqualification Proceedings
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Clinical Investigators - Disqualification Proceedings


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   No. of Records Found:  230
Name Center Status Date of status Date NIDPOE Issued Date NOOH Issued Link to NIDPOE Letter Link to NOOH Letter
Doss, Jr., William L., MD CDER Disqualified 06/14/1979 11/15/1977 03/03/1978
Chaplan, Abraham A., MD CDER Disqualified 02/28/1979
Lamphier, Timothy A., MD CDER Disqualified 02/14/1979
Dalton, Fred C., MD CDER Disqualified 01/03/1979 10/18/1978
Kurland, Morton L., MD CDER Disqualified 11/06/1978
Savery, Francois, MD CDER Disqualified 10/06/1978
Close, John H., MD CDER Disqualified 07/19/1978
Schneyer, Jerome J., MD CDER Disqualified 04/16/1978
McCracken, Elbert, MD CBER Disqualified 05/03/1977 07/12/1976 10/27/1976
Froning, Edward C., MD CDER Disqualified 04/10/1976 07/31/1975
Rotstein, Jerome, MD CDER Disqualified 12/03/1975
Day, Phillip L., MD CDER Disqualified 08/28/1975
Balin, Howard, MD CDER Disqualified 03/19/1975
Dunlop, Edwin, MD CDER Reinstated 12/24/1970
Sobatka, Joseph H., MD CDER Disqualified 09/21/1970
Shubin, Harry, MD CDER Disqualified 03/16/1970
Rubin, Wallace, MD CDER Disqualified 03/13/1970
Carter, Charles, MD CDER Reinstated 07/29/1969
Lapolla, Anthony, MD CDER Disqualified 05/05/1969
Bender, Sheldon R., MD CDER Disqualified 02/17/1969
McHardy, Gordon, MD CDER Reinstated 01/27/1969
Splitter, Samuel, MD CDER Disqualified 07/29/1968
Lowe, Leo, MD CDER Disqualified 10/18/1966
Abruzzi, Jr., William A., MD CDER Disqualified 08/31/1966
Copelan, Herbert W., MD CDER Reinstated 08/19/1966
Kligman, Albert M., MD CDER Reinstated 08/19/1966
Cass, Leo, MD CDER Disqualified 12/15/1965
Roberts, Kathleen E., MD CDER Disqualified 11/24/1964
Robin, Bennett, MD CDER Disqualified 06/19/1964
Kumar, Anil, MD CDER Not Disqualified 05/02/2014 PDF

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1.Under regulations in effect until 1987, investigators who met the standard for disqualification (repeated or deliberate failure to comply with applicable requirements) could potentially avoid disqualification and continue to be eligible to receive investigational products if they could provide FDA with adequate assurances of future compliance with requirements applicable to the use of investigational drugs and biologics. The provisions for adequate assurances are no longer in the regulations.

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