Drug Development Meetings
Join FDAnews Thursday, April 14, to hear Lisa Olson of SEC Associates explain what the FDA expects from computer systems you use to support your ongoing clinical studies at the "Computer Compliance for Clinical Trials: What FDA Expects in Adverse Event Reporting and Study Closure." Also learn from Lisa Olson April 28 at the FDAnews audioconference on "Computer Compliance for Clinical Trials: What FDA Expects for Recordkeeping and Archiving." Get up to date on what the FDA expects for computer systems used in study recordkeeping and archiving, the last phase in clinical trials.
April 11-12: Fourth International Metabolic Diseases Drug Discovery World Summit
San Diego, Calif.
(212) 967-0095
Strategic Research Institute
sgrodsky@srinstitute.com
www.srinstitute.com/cs325
April 11-12: Safety Neuropharmacology
Washington, D.C.
(831) 465-2295
Pharmaceutical Education Associates
jmcginnis@pharmedassociates.com
www.pharmedassociates.com
April 11-12: The Off-Label Crisis Workshop
Identify and Eliminate Risky Practices Before It's Too Late
Scottsdale, Ariz.
(703) 538-7600
FDAnews
www.fdanews.com/wbi/conferences/offlabelcrisis.html (http://www.fdanews.com/wbi/conferences/offlabelcrisis.html)
April 11-12: Third Annual Psychiatric Drug Discovery and Development
Princeton, N.J.
(212) 967-0095
Strategic Research Institute
sgrodsky@srinstitute.com
www.srinstitute.com/cs330
April 11-13: Biologics Drug Development: An Integrated Overview of Manufacturing, Nonclinical, Clinical and Regulatory Requirements
Washington, D.C.
(703) 276-0178
Peri
maria.simonetti@peri.org
www.peri.org
April 11-13: Pharmacogenomics in Drug Development and Regulatory Decisionmaking
North Bethesda, Md.
(215) 442-6100
DIA
dia@diahome.org
www.diahome.org/Content/Events/05013.pdf
April 13-15: Auditing and Inspecting Preclinical Research for GLP Compliance
New Brunswick, N.J.
(732) 238-1600
The Center for Professional Advancement
info@cfpa.com
www.cfpa.com
April 14: Computer Compliance for Clinical Trials
What FDA Expects in Adverse Event Reporting and Study Closure
An audioconference
Your Office
(703) 538-7600
FDAnews
www.fdanews.com/wbi/conferences/computer2.html (http://www.fdanews.com/wbi/conferences/computer2.html)
April 14-16: Preparation, Packaging and Labeling of Clinical Trial Materials
New Brunswick, N.J.
(732) 238-1600
The Center for Professional Advancement
info@cfpa.com
www.cfpa.com
April 18-19: Fundamentals of Biochemistry: Background for Biotechnology
New Brunswick, N.J.
(732) 238-1600
The Center for Professional Advancement
info@cfpa.com
www.cfpa.com
April 18-19: RNAi in Vivo
London, England
+44 207 647 2325
marcus evans Life Sciences
olas@marcusevansuk.com
www.melifesciences.com
April 18-19: Seventh International Neurodegeneration in Alzheimer's Disease, Parkinson's Disease and Related Disorders
Princeton, N.J.
(212) 967-0095
Strategic Research Institute
sgrodsky@srinstitute.com
www.srinstitute.com/cs331
April 18-19: Writing and Implementing Clinical Protocols
New Brunswick, N.J.
(732) 238-1600
The Center for Professional Advancement
info@cfpa.com
www.cfpa.com
April 18-20: Project Management in the Research-Based Pharmaceutical Industry
San Diego, Calif.
(703) 276-0178
Peri
maria.simonetti@peri.org
www.peri.org
April 19: Innovate or Stagnate
How to Generate Breakthrough Ideas for Quality Control and Continuous Improvement
An audioconference
Your Office
(703) 538-7600
FDAnews
www.fdanews.com/wbi/conferences/innovate.html (http://www.fdanews.com/wbi/conferences/innovate.html)
April 19-20: Adverse Drug Events -- Understanding and Reporting Requirements
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation & Education
info@cfpie.com
www.cfpie.com
April 20-21: Designing and Writing High Quality Clinical Study Protocols
Somerset, N.J.
(801) 685-7717 x306
McCulley/Cuppan
jgregg@mcculley-cuppan.com
www.mcculley-cuppan.com
April 20-22: CHI's Inaugural Preclinical Development
San Francisco, Calif.
(617) 630-1300
Cambridge Healthtech Institute
chi@healthtech.com
www.healthtech.com
April 21-22: Risk-Based Approach to Computer Compliance Focusing on Clinical Trials
Boston, Mass.
(919) 531-5369
SEC Associates and SAS
Dori.Pyles@SAS.com
http://support.sas.com/training/us/crs/bracc.html