Drug Development Meetings
Join FDAnews Tuesday, Oct. 31, for "Adaptive Clinical Trial Design: How to Lower Costs and Shorten Product Development Cycles." In this 90-minute interactive audioconference, Jerald S. Schindler, Dr.PH, president of Cytel Pharmaceutical Research Division, will explain how these trials can provide more information on a drug's efficacy, how they can result in a more ethical trial, how they can rescue a drug and how all this can be done without compromising the integrity of a trial. On Nov. 6, join FDAnews for "Proactive Planning for Recalls." In this 90-minute audioconference with Q&A session, noted attorney and author James M. Wood will share his proactive plan -- developed from real-world lessons he's learned during 30 years representing prescription medicine and medical device manufacturers -- on matters ranging from product recalls to off-label and liability issues.
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
Nov. 27-29: Auditing and Inspecting Preclinical Research for GLP Compliance
Amsterdam, The Netherlands
(732) 238-1600
The Center for Professional Advancement
asloane@cfpa.com
www.cfpa.com
Nov. 27-Dec. 1: Pharmacovigilance Training: Clinical Trials and Marketed Products
Paris, France
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
Nov. 29-30: European Filing and Registration Procedures
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=031&source=fdanewsconferencecalendarfree
Dec. 5-7: Generic Drug Approvals - Preparing an ANDA for First Cycle Approval
Malvern, Pa
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=038&source=fdanewsconferencecalendarfree
Dec. 5-7: The Quest to Enable the Electronic Clinical Trial: Finding Clarity in a Confusing World
Baltimore, Md.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
Dec. 6-7: The CTD Practical Implementation of the ICH Common Technical Document Format for Market Applications
Dublin, Ireland
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=078&source=fdanewsconferencecalendarfree
Dec. 7-8: Patient Registry Programs
Boston, Mass.
(703) 310-2549
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Dec. 18-19: Introduction to Clinical Data Management
Edison, N.J.
(703) 310-2549
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Dec. 18-20: Monitoring Clinical Drug Studies: Beginner
Boston, Mass.
(703) 310-2549
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Jan. 14-18, 2007: 6th Annual DIA Conference for Contemporary Pharmacovigilance and Risk Management Strategies
Washington, D.C.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
March 19-21, 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