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Mar 02, 2010DIA/FDA/PVRI Debate on Clinical Trials for Pulmonary Arterial HypertensionNorth Bethesda
Mar 14, 201021st Annual Workshop on Medical Communications: Defining the Future of Medical CommunicationsScottsdale
Mar 22, 2010DIA/FDA CDER/CBER Computational Science Annual MeetingNorth Bethesda
Mar 23, 20103rd Oligonucleotides-based Therapeutics ConferenceBethesda
Mar 23, 2010Evidence-based Medicine & Health Technology Assessment: Moving From Separate Appraisals to Synergistic CommunicationsWASHINGTON
Mar 26, 2010FDA Guidance on Adaptive Design for Clinical TrialsSilver Spring
Apr 11, 2010Cardiovascular Safety in Drug Development: QT, Arrhythmias, Thrombosis, and BleedingArlington
Apr 12, 2010Clinical Development of Stem Cell Therapies: Scientific, Regulatory and Ethical ConsiderationsNorth Bethesda
Apr 18, 20104th Annual FDA/DIA Statistics ForumNorth Bethesda
Jun 13, 201046th DIA Annual MeetingWashington
Sep 30, 2010Global Approach to the Risk Management of MedicinesWashington
Oct 05, 2010Development of Type 2 Diabetes Mellitus Drugs: State of the Art Cardiovascular Safety AssessmentsWashington
Oct 12, 2010Advancing Pediatric Research in the USBethesda
Oct 13, 2010Early Drug Development: Navigating the Treacherous RapidsBethesda
Oct 13, 2010Investing in Biomedical Informatics for Drug Development and Health CareNational Harbor
Oct 13, 2010Maternal and Pediatric Drug Safety SymposiumBethesda
Oct 14, 2010Partnerships to Advance Patient Recruitment and Retention in Clinical ResearchRockville
Oct 26, 2010Ensuring Quality and Balancing Risks for Multiregional Clinical Trials: Statistical, Clinical, Regulatory, and Ethical FactorsBethesda
Oct 26, 2010Tomorrow's Project Manager: Evolving Competencies for Biopharmaceutical ProfessionalsBethesda
Oct 28, 2010The 9th Annual Electronic Submissions Conference: Working Together Towards a Global StrategySan Diego
Nov 04, 2010DIA/FDA Orphan Drug Designation Workshop Lansdowne
Nov 04, 2010DIA’s 8th Annual Canadian Meeting: Fostering Innovation and Access to DrugsOttawa
Nov 09, 2010Sustaining Clinical Trial DisclosureBethesda
Nov 10, 20107th Latin American Congress of Clinical Research: Harmonization and the Future of Drug Development in Latin AmericaSão Paulo
Dec 08, 2010US and International Prescription Drug Labeling: Comparisons and Important UpdatesWashington
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10006 21st Annual Workshop on Medical Communications: Defining the Future of Medical Communications
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Title:
21st Annual Workshop on Medical Communications: Defining the Future of Medical Communications


Date(s) And Time(s):
Mar 14 2010 8:00AM - Mar 17 2010 5:00PM

Location:
JW Marriott Camelback Inn Resort & Spa
5402 E. Lincoln Drive
Scottsdale, AZ 85253 

Interest Area(s):
Medical Communications,Medical Writing,Regulatory Affairs,Clinical Research

Overview:

Nine exciting, interactive breakout sessions on topics essential to medical information, medical liaisons, and contact centers

 

Preworkshop Highlights
Sunday, March 14
• Core Curriculum – Full-day session 8:00 AM-4:30 PM
Separate registration is required.

This program is specifically designed to meet the needs of individuals new to pharmaceutical industry-based medical communications. Those who have been in this function for less than 1 year would gain the most from attending.
• Afternoon Tutorials – 1:30-5:00 PM
Separate registration is required.
– Medical Science Liaisons
– Literature Searching/Medical Writing
– Evidence-based Medicine
– Practical Applications of Biostatistics

Workshop Highlights
Monday, March 15
• Opening Session – Health Care Reform Update
• Appropriate data sources: Evidence-based medicine versus alternative sources
• Breakout sessions for field-based medical liaisons (interactions with academia and MSL 2009 survey results), contact center (handling of product recalls, and emerging technology), and headquarters-based medical communications (sharing information between companies, and promotional review)
• Welcoming reception featuring speed networking
Tuesday, March 16
• The future of medical communications
• Leadership and professional development
• Podium and poster pearls
• Breakout sessions on customer insights, compliance, and sales training
• Evening reception featuring professional poster presentations

Wednesday, March 17
• Regulatory Review
• Medical communications experience with Risk Evaluation and Mitigation Strategy (REMS)



Learning Objectives:

At the conclusion of this workshop, participants should be able to:

·      Demonstrate core competencies in industry-based drug information practice for both field-based and headquarter-based; verbal and written responses; provision of on-label and off-label information; medical and scientific literature evaluation; regulatory and legal applications; and scientific balance versus fair balance

·      Discuss important and recent developments regarding health care reform and regulatory guidance related to medical communications

·      Recognize medical communications involvement in job functions such as promotional review, REMS, training, compliance, and referencing

·      Assess the current landscape for field-based medical communications, and identify ways to enhance their ability to interact with academicians

·      Discuss the do’s and don’ts of dissemination of off-label information

·      Identify obstacles and opportunities on the horizon for medical communications, and potential ways to benefit from both



Target Audience:

Professionals who work in the following areas:

·      Medical communications

·      Medical liaisons

·      Medical information

·      Medical call center environment

·      Industry, academia, and government



Event Code:
10006

Contact Information:

WORKSHOP INFORMATION

Contact JoAnn Boileau, Program Manager, Phone +1.215.442.6175, Fax +1.215.442.6199, or email JoAnn.Boileau@diahome.org