Drug Development Meetings

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Join FDAnews Monday, April 24 for a 90-minute audioconference, "Adverse Event Compliance in Clinical Trials: Know What to Report, When and How." Expert Mark Barnes will help demystify adverse event reporting for your clinical trials. On April 25, join FDAnews for "Out-of-Specification Results and Failure Investigations: How Science Should Drive Your Compliance." In this 90-minute audioconference with Q&A session, compliance expert and former industry quality director Gordon Richman will show you how to use a scientific focus in your investigations to deliver improved product quality, speed time to market and reduce compliance-related costs.

April 24: Adverse Event Compliance in Clinical Trials Know What to Report, When and How An audioconference Your Office (703) 538-7600 www.fdanews.com/wbi/conferences/aecompliance.html (http://www.fdanews.com/wbi/conferences/aecompliance.html)

April 24-25: Introduction to Clinical Data Management Boston, Mass. (610) 548-2200 Barnett Educational Services customer.service@parexel.com www.barnettinternational.com/index-flash.html

April 24-25: Standard Operating Procedures (SOPs) in Clinical Research San Francisco, Calif. (610) 548-2200 Barnett Educational Services customer.service@parexel.com

www.barnettinternational.com/index-flash.html

May 1-2: Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA Dublin, Ireland (610) 688-1708 The Center for Professional Innovation and Education info@cfpie.com www.cfpie.com/showitem.aspx?productid=085&source=fdanewsconferencecalendarfree

May 1-3: Auditing & Inspecting Preclinical Research for GLP Compliance Millbrae, Calif. (732) 238-1600 Center for Professional Advancement info@cfpa.com

www.cfpa.com

May 4-5: Project Management in Drug Development: Phase I and Phase II Clinical Development Research Triangle Park, N.C. (212) 661-3250 PTi international.com dweinberg@pti-international.com www.pti-international.com

May 8-10: Generic Drug Approvals Amsterdam, the Netherlands 31 20 638 28 06 Center for Professional Advancement amsterdam@cfpa.com www.cfpa.com

May 9-10: How to Monitor Clinical Trials for GCP Compliance Dublin, Ireland

(610) 688-1708 The Center for Professional Innovation and Education info@cfpie.com

www.cfpie.com/showitem.aspx?productid=043&source=fdanewsconferencecalendarfree

May 11-12: Complying with the EU Clinical Trial Directive Morristown, NJ (212) 661-3250 PTi international dweinberg@pti-international.com www.pti-international.com

May 15-17: Non-clinical Drug Safety Evaluation & Drug Development Amsterdam, the Netherlands 31 20 638 28 06 Center for Professional Advancement amsterdam@cfpa.com

www.cfpa.com

May 21-24: Outsourcing & Offshoring Clinical Trials

Boston, Mass. (773) 695-9400 Advanced Learning Institute bob@aliconferences.com

www.aliconferences.com

May 22-23: Complying with the EU Clinical Trial Directive Washington, DC (212) 661-3250 PTi international

dweinberg@pti-international.com www.pti-international.com