FDAnews
www.fdanews.com/articles/68861-drug-development-meetings

Drug Development Meetings

February 17, 2005

Join FDAnews Feb. 24 to learn about "Drug Marketing Practices in Europe: Navigating Tough Rules and New Enforcement," a 90-minute audioconference. Hear former FDA official Linda Horton, now an attorney with Hogan & Hartson, explain how the new EU Community Code on Medicinal Products affects your marketing activities, including your relationship with health professionals. On Feb. 25, receive a concise and expert analysis of the "Medicare Part D for Drugmakers: New Requirements, New Risks, New Markets," presented in a 90-minute audioconference by Keith Korenchuk of McGuireWoods and Sheryl Vacca of Deloitte & Touche.

Feb. 23: cGMP Predicate Rules

What FDA Expects From Your Computer Systems

Part 2 of a 2-Part Series

An audioconference

Your Office

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/gmprules2.html (http://www.fdanews.com/wbi/conferences/gmprules2.html)

Feb. 24: Drug Marketing Practices in Europe

Navigating Tough Rules and New Enforcement

An audioconference

Your Office

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/eurules.html (http://www.fdanews.com/wbi/conferences/eurules.html)

Feb. 24-25: Auditing Clinical Trials for GCP Compliance

New Brunswick, N.J.

(212) 661-3500 x3091

PTi international

jmcconnell@pti-international.com

www.pti-international.com

Feb. 24-25: Project Management for Clinical Trials

San Francisco, Calif.

(212) 661-3500

PTi international

jmcconnell@pti-international.com

www.pti-international.com

Feb. 25: Medicare Part D for Drugmakers

New Requirements, New Risks, New Markets

An audioconference

Your Office

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/medicarepartd.html (http://www.fdanews.com/wbi/conferences/medicarepartd.html)

Feb. 28: Preparing for Systems-Based Inspections

An audioconference with Martin Browning

Your Office

(703) 538-7600

FDAnews

www.fdanews.com/wbi/conferences/inspections.html (http://www.fdanews.com/wbi/conferences/inspections.html)

Feb. 28-March 1: Implementing the Common Technical Document Format for NDA/BLA Submissions

Washington, D.C.

(212) 661-3500 x3091

PTi international

jmcconnell@pti-international.com

www.pti-international.com

Feb. 28-March 1: Third International Protein Phosphorylation Drug Discovery World Summit

La Jolla, Calif.

(646) 336-7030

Strategic Research Institute

sgrodsky@srinstitute.com

www.srinstitute.com

March 2-3: Project Management in Drug Development: Discovery and Preclinical

Philadelphia, Pa.

(212) 661-3500

PTi international

jmcconnell@pti-international.com

www.pti-international.com

March 2-4: INDs and NDAs and FDA Regulations

Amsterdam, Netherlands

(732) 238-1600

The Center for Professional Advancement

info@cfpa.com

www.cfpa.com

March 4: The Impact of the EU Clinical Trials Directive on the Clinical Supply Chain and Clinical Manufacturing Facilities

Rome, Italy

(301) 656-5900

PDA

tri@pda.org

www.pda.org

March 4: cGMP and Other Regulatory Compliance During Development of Biopharmaceuticals and Biologics

Malvern, Pa.

(610) 688-1708

The Center for Professional Innovation & Education

info@cfpie.com

www.cfpie.com