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09103 3rd Annual Clinical Forum
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Title:
3rd Annual Clinical Forum


Date(s) And Time(s):
Oct 19 2009 9:00AM - Oct 21 2009 1:00PM

Location:
Nice Acropolis
1, Esplanade Kennedy
BP 4083
06302 Nice
France

Interest Area(s):
CMC, Clinical Safety/Pharmacovigilance, Clinical Research, Medical Communications, Medical Writing, Nonclinical, Outsourcing, Project Management, Quality Assurance/Quality Control, Regulatory Affairs, Research & Development, Statistics

Overview:

Dear Colleagues,

We all strive for optimal performance and efficiency in our different positions in clinical drug development and many achievements have been made. Collectively, however, our industry has not yet been able to consistently reduce time and costs of clinical development of new drugs. New challenges concerning novel development concepts lie ahead of us and need to be tackled.

The programme of the 3rd Annual Clinical Forum 2009 will be designed to update you on current experience, practices, approaches and concepts in your own disciplines and to develop new ideas for better processes by brainstorming and communicating with other disciplines and stakeholders involved in clinical research: “Improving Clinical Development Together!” is the motto for this conference.

The 3rd Annual Clinical Forum will host the Annual CDM, IT/Validation, Medical Information & Communications, Statistics and the Medical Writing conferences.

In informative sessions and interactive workshops we will cover “hot topics” in Clinical Operations and place special emphasis, in multi-disciplinary discussions, on practical aspects of the topics “non-interventional studies”, “trials with adaptive designs”, “trials with drugs for personalised treatment” and “possibilities to increase the efficiency of the industry - investigative site interface”. We will include workshops for your personal development needs.

With the many relevant and engaging topics to be covered, we hope that you will be interested in actively participating in the 3rd Annual Clinical Forum 2009 by providing us with your experience, case studies and best practices, described in abstracts for presentations by April 9, 2009.

Looking forward to welcoming you – as presenter or participant to Nice in October 2009.

Ingrid Klingmann
Programme Chairperson
Pharmaplex bvba
Belgium

Useful Links:
~ Call for Abstract Flyer
~ Registration form
~ Click here to submit your abstracts online

 



Target Audience:

Professionals at all levels in the following disciplines:
• Clinical Data Management
• eClinical
• Statistics
• Clinical Research
• Clinical Operations
• Post Marketing development
• Medical Information & Communications
• Clinical Safety & Pharmacovigilance
• Personal Development
• Validation
• Quality Assurance
• Medical Writing

Cancellation Policy

All cancellations must be in writing and be received at the DIA office by 17:00 CET on October 12, 2009

Cancellations received by the date above are subject to an administrative fee:

Full Meeting Cancellation: Member/Non-member = 200.00
Government/Academia/Non-profit (Member/Non-member) = 100.00.

Registrants who do not cancel by the date above and do not attend, will be responsible for the full registration fee. Registrants are responsible for cancelling their own hotel reservations. DIA reserves the right to alter the venue if necessary. If an event is cancelled DIA is not responsible for airfare, hotel or other costs incurred by registrants. Payment of registration fees must be received before commencement of the event.

Transfer Policy

You may transfer your registration to a colleague prior to the start of the event but membership is not transferable. Substitute registrants will be responsible for the non-member fee, if applicable. Please notify the DIA office of any such substitutions as soon as possible.



Event Code:
09103

Contact Information:
 

DIA EUROPE

ELISABETHENANLAGE 25, POSTFACH

4002 BASEL, SWITZERLAND

PHONE: +41 61 225 51 51

FAX: +41 61 225 51 52

E-MAIL: DIAEUROPE@DIAEUROPE.ORG