Drug Development Meetings
Join FDAnews Thursday, Sept. 7, for "Prepare Now for FDA Enforcement of Drug Pedigree Laws." In this 90-minute interactive audioconference, Eric F. Greenberg, principal attorney for the law firm of Eric F. Greenberg, P.C., tells you what drugs the FDA plans to focus on first, who must comply with the drug pedigree requirements, how the FDA plans to enforce the rule, whether you have to invest in expensive RFID technologies (and what problems RFID can cause) and more. On Sept. 12, join FDAnews for "Complying with New Cardiac Safety Guidelines for Clinical Trials: Best Practices for Conducting QT Tests." In this 90-minute audioconference with Q&A session, Daniel B. Goodman, M.D., director of medical affairs, Covance Cardiac Safety Services, hands you best practices for development and implementation of a reliable, cost-effective QT prolongation trial that meets the FDA's expectations.
Oct. 2-3: Planning for and Managing FDA GCP Inspections
San Francisco, Calif.
(800) 953-3398
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Oct. 3-5: Combination Product Development: Safety/Registration/Approval
East Brunswick, N.J.
(732) 238-1600
The Center for Professional Advancement
asloane@cfpa.com
www.cfpa.com
Oct. 4-6: Practical GCP Compliance Auditing of Trials & Systems
London, UK
(215) 442-6100
Practical GCP Compliance Auditing of Trials & Systems
dia@diahome.org
www.diahome.org
Oct. 4-6: Statistical Methodology in Clinical R&D
Heidelberg, Germany
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
Oct. 5: Overview for Regulatory Affairs Personnel on the Requirements for Submission of Clinical Data for NDAs
Online
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
Oct. 5-6: Conducting Clinical Trials in Developing Regions
Philadelphia, Pa.
(800) 953-3398
Barnett Educational Services
customer.service@parexel.com
www.barnettinternational.com
Nov. 1-2: CHI's Enhanced and Innovative Clinical Trial Design
Sheraton Centre Toronto, Toronto, Canada
(781) 972-5400
Cambridge Healthtech Institute
chi@healthtech.com
www.healthtech.com
Nov. 1-2: The CTD Practical Implementation of the ICH Common Technical Document Format For Market Applications
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation and Education
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=078&source=fdanewsconferencecalendarfree
Nov. 16-17: Drug Development in India
Boston, Mass.
(617) 630-1300
Cambridge Healthtech Institute
chi@healthtech.com
www.healthtech.com
Dec. 4-5: Electronic Patient Reported Outcomes (ePRO) Update: The Quest to Move from Paper to Plastic
Baltimore, Md.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
Dec. 4-6: Advanced Topics in Clinical Research/Drug Development
Scottsdale, Ariz.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org
March 18-20: 22nd Annual DIA CLINICAL DATA MANAGEMENT Symposium and Exhibition Integration Across the Clinical Trial Continuum
Hilton in the Walt Disney World, Lake Buena Vista, Fla.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org