Drug Development Meetings
Join FDAnews Tuesday, Sept. 12, for "Complying with New Cardiac Safety Guidelines for Clinical Trials: Best Practices for Conducting QT Tests." In this 90-minute interactive audioconference, Daniel B. Goodman, M.D., director of medical affairs, Covance Cardiac Safety Services, hands you best practices for development and implementation of a reliable, cost-effective QT prolongation trial that meets the FDA's expectations. On Sept. 21, join FDAnews for "Reduce cGMP Inspections: Lower Your Site Risk Potential (SRP) Score." In this 90-minute audioconference with Q&A session, Justin O. Neway, Ph.D., vice president and chief science officer, Aegis Analytical Corp., hands you proven strategies to reduce SRP scores.
Oct. 9-10: Advanced GCP Compliance
Philadelphia, Pa.
(800) 953-3398
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Oct. 9-10: The CRA Manager Course
Chicago, Ill.
(800) 953-3398
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Oct. 9-11: Drug Discovery to Clinical Trials
Mumbai, India
+65 68355 107
IBC Life Sciences
Lynn.Ng@ibcasia.com.sg
www.drugdisc.com/india
Oct. 9-11: Generic Drug Approvals - Preparing an ANDA for First Cycle Approval
Dublin, Ireland
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=038&source=fdanewsconferencecalendarfree
Oct. 9-Nov. 10: Statistical Concepts for Non-Statisticians
Boston, Mass.
(800) 953-3398
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Nov. 8: High Quality Investigation Reporting
Webinar
(801) 685-7717
McCulley/Cuppan LLC
jmahajan@mcculley-cuppan.com
www.mcculley-cuppan.com
Nov. 27: Achieving & Maintaining 21 CFR Part 11 Compliance
Princeton, N.J.
(215) 354-1720
Validation Associates, Inc.
info@validassoc.com
www.validassoc.com
Nov. 27-28: The EU Clinical Trial Directive
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=030&source=fdanewsconferencecalendarfree
Dec. 11-13: Drug Product Stability and Shelf-Life
Milbrae, Calif.
(732) 238-1600
The Center for Professional Advancement
asloane@cfpa.com
www.cfpa.com
Dec. 11-13: The Drug Development Process - From Discovery to Commercialization
Irvine, Calif.
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=025&source=fdanewsconferencecalendarfree
Dec. 13-15: EudraVigilance: Electronic Reporting of ICSRs in the EEA
London, UK
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
March 18-20, 2007: 22nd Annual DIA CLINICAL DATA MANAGEMENT Symposium and Exhibition Integration Across the Clinical Trial Continuum
Hilton in the Walt Disney World, Lake Buena Vista, Fla.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org