FDAnews
www.fdanews.com/articles/96657-drug-development-meetings

Drug Development Meetings

August 2, 2007

On Tuesday, August 14, join FDAnews for “Negotiating Corporate Integrity Agreements.” In this 90-minute audioconference, Jesse Witten will share successful strategies that show you how to comply with HHS reimbursement requirements while saving time and money. On Wednesday, August 15, join FDAnews for “New State False Claims Acts: 19 Different Sets of Laws and More on the Way.” In this 90-minute audioconference, attorneys Keith Korenchuk and Rebecca Rohr will compare state false claims acts with the federal statute, detailing where the state laws are tougher than federal law and the requirements that are unique. Then, on Thursday, August 16, join FDAnews for “Clinical Trials in the Developing World: An On-the-Ground Look at Risks and Best Practices.” In this 90-minute audioconference, Clint Hermes will explore the benefits and risks of conducting clinical trials in developing countries.

On Tuesday, August 21, join FDAnews for “EudraVigilance Deconstructed: Submitting Compliant EU Adverse Event Reports.” In this 90-minute audioconference, A. Michael Bloh will provide guidance on the confusing registration process as well as define and explain many of the unfamiliar terms and acronyms in EudraVigilance documentation.

Tuesday, Aug. 7 - Wednesday, Aug. 8, 2007
The EU Clinical Trial Directive
Costa Mesa, Calif.
(610) 688-1708
The Center for Professional Innovation & Education (CfPIE)
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=030&source=fdancc

Thursday, Aug. 9 - Friday, Aug. 10, 2007
European Filing & Registration Procedures
Costa Mesa, Calif.
(610) 688-1708
The Center for Professional Innovation & Education (CfPIE)
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=031&source=fdancc

Thursday, Aug. 9 - Friday, Aug. 10, 2007
Writing and Implementing Clinical Protocols
New Brunswick, N.J.
(732) 238-1600
The Center for Professional Advancement
salbers@cfpa.com
www.cfpa.com

Wednesday, Aug. 22 - Friday, Aug. 24, 2007
Good Clinical Practices
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation & Education (CfPIe)
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=039&source=fdancc

Wednesday, Sept. 5 - Friday, Sept. 7, 2007
Non-Clinical Drug Safety Evaluation and Drug Development
Millbrae, Calif.
(732) 238-1600
The Center for Professional Advancement
info@cfpa.com
www.cfpa.com/template_courses.asp?course_name=200709051153-11a

Thursday, Sept. 13 - Saturday, Sept. 15, 2007 
World Cancer Conference
Beijing, China
(011) 8621.5282
IBC Shanghai
talli.hu@ibcchina.com.cn
www.ibcchina.com.cn/worldcancer

Monday, Sept. 17 - Wednesday, Sept. 19, 2007 
Fundamentals of Clinical Research Monitoring Training Course
Philadelphia, Pa.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org

Thursday, Sept. 20 - Friday, Sept. 21, 2007 
Drug/Device Combinations - Practical Guidance on Borderline Issues & Combination Products
London, UK
(148) 373-0071
Management Forum Ltd
info@management-forum.co.uk
www.management-forum.co.uk

Tuesday, Oct. 2 - Wednesday, Oct. 3, 2007 
Drug Discovery: The Application of High-Throughput Technologies to Target and Lead Identification
Nothingham, UK
(203) 743-1336
Society for Biomolecular Sciences
mmanoni@sbsonline.org
www.sbsonline.org/events/symposia/elrig_2007/index.php

Thursday, Oct. 4 - Friday, Oct. 5, 2007 
“Fear No Yellow Stickies:” Entry Level Coordinator Training
Orlando, Fla.
(701) 426-9034
Aureus Research Consultants
jenniferd@aureusresearch.com
www.aureusresearch.com

Thursday, Nov. 1 - Friday, Nov. 2, 2007 
FDA Inspections of Clinical Data Systems
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation & EducationCfPIE
info@cfpie.com
www.cfpie.com/showitem.aspx?productid=034&source=fdancc

Monday, Nov. 5, 2007 
Regulatory Affairs: Part I : The IND Phase & Part II: The CTD/NDA Phase
Philadelphia, Pa.
(215) 442-6100
Drug Information Association
dia@diahome.org
www.diahome.org