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B.R.I.D.G.E. TO DATA®

PERI, Inc.

"Kidz with Leukemia: A Space Adventure"

"Conquering Cancer Network"

Judith K. Jones, MD, PhD

President and Founder

  • Former FDA Safety Director

  • Internationally-recognized authority in:

  • Adverse Drug Reactions

  • Pharmacoepidemiology

  • Drug Development

  • Drug Regulation

  • Risk Management

Dr. Judith K. Jones is a clinical pharmacologist,  pharmacoepidemiologist, and geriatrician/internist with a long-standing interest in the study of adverse drug reactions, drug utilization, and drug development and regulation. She received her medical training at Baylor College of Medicine in Houston, Texas, followed by clinical training, a fellowship in clinical pharmacology and a PhD in developmental pharmacology at University of California at San Francisco.

In the 1970' s, interested in the translation of basic pharmacology information to the practice site, Dr. Jones practiced, taught clinical pharmacology and carried out early research in drug utilization at Pacific Medical Center in San Francisco. In 1978, she came to Washington, DC as Director of the FDA' s Division of Drug Experience (now Epidemiology) until 1984, and was then Special Asst. to the Director, Biometrics and Epidemiology through mid-1985.

Leaving the FDA, she returned to practice in 1985 in Medicine and Geriatrics at Georgetown University, where she continues as Associate Clinical Professor of Pharmacology. She is also Adjunct Professor of the Health Sciences at George Washington University, and is also Adjunct at the University of Michigan School of Public Health's Summer Program where she teaches a course in Pharmacoepidemiology.

In 1988, she founded The Degge Group, Ltd., a consulting business that provides services relating to drug safety information, regulation, research and education. Dr. Jones also serves as President of the Pharmaceutical Education and Research Institute, Inc. (PERI) that was founded in 1989 by PhRMA .

Dr. Jones has published a number of articles relating to adverse reactions, post-marketing surveillance of drugs, pharmaceutical risk management, drugs in geriatric patients, and drug information for patients and physicians.

 

The Degge Group, Ltd.

Consulting in clinical drug safety, pharmacovigilance, and pharmacoepidemiology since 1988.

1616 North Fort Myer Drive, Suite 1430
Arlington, Virginia 22209 USA
1 (888) 413-3443
Phone: +1 (703) 276-0067 || Fax: +1 (703) 276-0069

 

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