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. 15-17: Reporting Failure Investigations and Process Deviations
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=068&source=fdanewsconferencecalendarfree
Nov. 15-18: 2006 Annual Human Research Protection Programs (HRPP) Conference
Marriott Wardman Park Hotel, Washington, D.C.
(617) 423-4112
Public Responsibility in Medicine and Research (PRIM&R)
broskin@primr.org
www.primr.org
Nov. 16-17: Drug Development in India
Boston, Mass.
(617) 630-1300
Cambridge Healthtech Institute
chi@healthtech.com
www.healthtech.com
Nov. 16-17: Stability Programs from Development to Approval
Dublin, Ireland
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=072&source=fdanewsconferencecalendarfree
Nov. 30-Dec. 1: Clinical Project Management: Introduction
San Diego, Calif.
(703) 310-2549
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Nov. 30-Dec. 1: Monitoring Clinical Drug Studies: Intermediate
Chicago, Ill.
(703) 310-2549
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Nov. 30-Dec. 1: Regulatory and Clinical Considerations in the Development of Combination Products
San Diego, Calif.
(703) 310-2549
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Nov. 30-Dec. 1: Standard Operating Procedures (SOPs) in Clinical Research
Boston, Mass.
(703) 310-2549
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Dec. 13-15: EudraVigilance: Electronic Reporting of ICSRs in the EEA
EMEA, Canary Wharf, London, UK
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
Dec. 14-15: How to Prepare for a Systems-based Inspection -- Understanding FDA's Risk-Based Inspections Approach
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=094&source=fdanewsconferencecalendarfree
Jan. 22-23, 2007: Good Clinical Practices for Research Professionals
Orlando, Fla.
(813) 264-0863
Research Dynamics Consulting Group, Ltd.
klongley@resdyncg.com
www.resdyncg.com
Jan. 24-25, 2007: Sharing Data and Models to Improve Clinical Drug Development and Regulatory Decisions
Washington Marriott Hotel, Washington, D.C.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org