In February 1999 CDDS sponsored a meeting "Modeling and Simulation of Clinical Trials: Best Practices Workshop" to develop suggestions for good practices in the use of modeling and simulation.
A first version of a document describing the outcome of this meeting has been completed:
Simulation in Drug Development: Good Practices
Editors: Holford NHG, Hale M, Ko HC, Steimer J-L, Sheiner LB, Peck CC Contributors: Bonate P, Gillespie WR, Ludden T, Rubin DB, Stanski D
We consider this document to be dynamic and improvable, so we look forward to receiving feedback from readers. Special attention will be given to commentaries that reflect evaluation of the proposed practices after good faith attempts to implement them. We suggest December 31, 1999 as a closing date for feedback to the manuscript.
Please direct comments to:
Nick Holford, Dept Pharmacology & Clinical Pharmacology
University of Auckland, Private Bag 92019, Auckland, New Zealand
email: n.holford@auckland.ac.nz tel:+64(9)373-7599 x 6730 fax:373-7556
Carl Peck
Director
Center for Drug Development Science
Georgetown University Medical Center
tel: 202-687-4332
fax: 202-687-0193
Improving Drug Development Using Patient Adherence Data
in Clinical Trials, May 6-7, 2008.
Brochure (PDF)
Registration site
Advanced NONMEM workshop – March 17–19, 2008 at Mission Bay Conference Center, San Francisco, CA.
More information >
UCSF-CDDS to launch The American Course on Drug Development and
Regulatory Science- September 2007
More information >
CDDS – Pharmacometric Services is available to drug researchers
More >
Howard Lee, MD, PhD, named Director of CDDS
More >
Lewis B. Sheiner Memorial. Symposium held at CDDS in December 2006
More >
This site will look much better in a browser that supports web standards, but it is accessible to any browser or Internet device. Please upgrade your browser.