Drug Development Meetings

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Join FDAnews Wednesday, April 19 for a 90-minute audioconference, "Writing and Enforcing Effective SOPs: Avoid Regulatory Action and Improve Efficiency." Expert Annalisa Pizzarello will walk you through some of the basic guidelines for making sure your company effectively documents its processes and consistently follows them, helping you to avoid regulatory action and increase efficiency. On April 24, join FDAnews for "Adverse Event Compliance in Clinical Trials: Know What to Report, When and How." In this 90-minute audioconference with Q&A session, expert Mark Barnes will help demystify adverse event reporting for your clinical trials.

April 17-18: Introduction to Clinical Project Management San Francisco, Calif. (610) 548-2200 Barnett Educational Services customer.service@parexel.com www.barnettinternational.com/index-flash.html

April 20-21: Auditing Techniques for Clinical Research Professionals Boston, Mass. (610) 548-2200 Barnett Educational Services customer.service@parexel.com

www.barnettinternational.com/index-flash.html

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

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