FDAnews
www.fdanews.com/articles/63259-drug-development-meetings

Drug Development Meetings

October 12, 2006

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 for product recalls -- 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. 13-14: CGMPs for the Biotechnology and Pharmaceutical Industries

Seattle, Wash.

(443) 543-5532

SPI USA Inc.

nhawkins@usaspi.com

www.usaspi.com

Nov. 13-14: Clinical Project Management: Introduction

Boston, Mass.

(703) 310-2549

Barnett Educational Services

customer.service@parexel.com

www.barnettinternational.com

Nov. 13-14: Good Clinical Practices for Research Professionals

Las Vegas, Nev.

(813) 264-0863

Research Dynamics Consulting Group, Ltd.

klongley@resdyncg.com

www.resdyncg.com

Nov. 13-14: Good Laboratory Practice for Pre-Clinical Testing, Compliance, QA and Audit

Malvern, Pa.

(610) 688-1708

The Center for Professional Innovation and Education

info@cfpie.com

www.cfpie.com/showitem.aspx?productid=040&source=fdanewsconferencecalendarfree

Nov. 13-14: Patient Recruitment and Retention

Chicago, Ill.

(703) 310-2549

Barnett Educational Services

customer.service@parexel.com

www.barnettinternational.com

Nov. 13-15: Regulatory II: The CTD/NDA Phase

Washington, D.C.

(215) 442-6100

Drug Information Association

dia@diahome.org

www.diahome.org

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: Conducting Clinical Trials Under ICH GCP

Chicago, Ill.

(703) 310-2549

Barnett Educational Services

customer.service@parexel.com

www.barnettinternational.com

Dec. 12-13: Pharmaceutical Fast Track

East Brunswick, N.J.

(732) 238-1600

The Center for Professional Advancement

asloane@cfpa.com

www.cfpa.com

Dec. 14-15: Effective Clinical Report Writing

Philadelphia, Pa.

(703) 310-2549

Barnett Educational Services

customer.service@parexel.com

www.barnettinternational.com

Jan. 14-18: 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