Bio-IT World Conference & Expo • April 20-22, 2010, World Trade Center •Boston, MA
Join more than 1,500 delegates from around the world to share information and enabling technologies driving biomedical research and drug development. Since 2002, the annual Bio-IT World Conference & Expo has established itself as the premier event showcasing the myriad applications of IT and informatics to biomedical research and the drug discovery enterprise. The 2010 program will feature best practice case studies and joint partner presentations relevant to the technologies, research, and regulatory issues of life science, pharmaceutical, clinical, and IT professionals.
The event features keynote presentations by John Halamka, M.D., M.S., Chief Information Officer, Harvard Medical School and Christoph Westphal, M.D., Ph.D., Chief Executive Officer, Sirtris Pharmaceuticals; Senior Vice President, Centre of Excellence for External Drug Discovery, GlaxoSmithKline.
Spanning three days, the meeting includes seven concurrent conference tracks dedicated to IT Infrastructure – Hardware, IT Infrastructure – Software, Bioinformatics, Systems Biology, Cheminformatics, eClinical Trials Technology, and eHealth Solutions.
Detailed information about the event can be found at the event website: www.bio-itworldexpo.com
The Post-Approval Summit • May 11-12, 2010 • Boston, MA
The Post-Approval Summit®, held at Harvard Medical School, focuses on strategies and best practices for demonstrating and improving the safety, effectiveness, value and quality of healthcare products and services through Phase IV studies, Patient Registries, Risk Management Programs and Quality Initiatives. Register today!
CHI Events
X Gen Congress • March 15-19, 2010 • San Diego, CA
Sequencing Data Analysis and Storage • March 15-17, 2010 • San Diego, CA
Epigenetics • March 15-17, 2010 • San Diego, CA
Comprehending Copy Number Variation • March 15-17, 2010 • San Diego, CA
Quantiative PCR • March 17-19, 2010 • San Diego, CA
Now-Generation Sequencing • March 17-19, 2010 • San Diego, CA
microRNA in Human Disease and Development • March 22-24, 2010 • Cambridge, MA
Alliance Management Congress • April 13-14, 2010 • Philadelphia, PA
Biopharmaceutical Change Control • April 13-15, 2010 • San Diego, CA
Combination Drug Therapies • April 13-14, 2010 • Philadelphia, PA
Future Diagnostics • April 26-27, 2010 • Irvine, CA
Drug Discovery Chemistry • April 27-29, 2010 • San Diego, CA
Fragment-Based Drug Discovery • April 27-28, 2010 • San Diego, CA
Antibacterial Drug Discovery • April 27-28, 2010 • San Diego, CA
Anti-inflammatories • April 27-28, 2010 • San Diego, CA
HCV Drug Discovery •April 28-29, 2010 • San Diego, CA
Kinase Inhibitor Chemistry • April 28-29, 2010 • San Diego, CA
Complete Event Listings
CHI Upcoming Short Courses
A Practical Guide to Finding Regions of Chromosomal Copy Number Gain or Loss • March 15-15, 2010 • San Diego, CA
Sequencing Data Storage • March 15, 2010 • San Diego, CA
Getting the Most out of Your Real-Time PCR Experiments • March 16, 2010 • San Diego, CA
microRNA Identification, Profiling and Validation Techniques • March 22, 2010 • Cambridge, MA
Building Effective Infrastructure for Alliance Management Execution • April 12, 2010 • Philadelphia, PA
Business Strategies for Companion Diagnostics • April 12, 2010 • Philadelphia, PA
Life Cycle Management of Pharmaceuticals and Biologics • April 12-12, 2010 • Philadelphia, PA
Biosimilars • April 14-14, 2010 • San Diego, CA
Life-Cycle Management of Pharmaceuticals and Biologics • April 13, 2010 • Philadelphia, PA
Micro and Nanofluidics in Diagnostics and Life Sciences • April 25, 2010 • Irvine, CA
The Impact of Outsourcing • April 26, 2010 • San Diego, CA
Fragment-Inspired Medicinal Chemistry • April 26, 2010 • San Diego, CA
Complete Short Course Listings
Barnett Educational Services
Barnett Web Seminars
Monitoring Reports: 10 Rules of Effective Report Writing • March 15, 2010
Essential Documentation in Clinical Trials at Research Sites • March 15, 2010
Subject Recruitment: Proactive Project Plans & Issues Management • March 16, 2010
HIPAA Team Training • March 17, 2010
Meeting International Safety Reporting Requirements • March 17, 2010
Critical Decision Points in Design & Conduct of Patient Registries • March 18, 2010
HIPAA Fact or Fiction: Current Practice Update for Clinical Research • March 18, 2010
Strategies for Managing Difficult Clinical Research Sites • March 19, 2010
Key Components of a Successful Study Site Start-up • March 22, 2010
Current Developments and Emerging Trends in the Role of IRBs • March 22, 2010
Navigating the FDA's New Website • March 23, 2010
Principal Investigator Training: Roles and Responsibilities • March 24, 2010
Investigational Product Accountability Training for Research Site Personnel • March 25, 2010
Managing CRAs to Improve Performance & Study Outcomes • March 26, 2010
Developing and Negotiating Research Site Clinical Study Budgets • March 29, 2010
Monitoring Informed Consent: The Process and Document • March 29, 2010
Trial Master File for Research Sites • March 30, 2010
CRC & PI Current Practice Update: Impact of the FDA BIMO Initiative • March 31, 2010
Complete Web Listings
Barnett Live Seminars
Drug Approval Process •March 16-17, 2010 • San Diego, CA
Introduction to Clinical Data Management •March 16-17, 2010 • San Diego, CA
Monitoring Clinical Drug Studies: Advanced •March 16-17, 2010 • San Diego, CA
Developing Clinical Study Budgets •March 18, 2010 • San Diego, CA
Source Documentation •March 18, 2010 • San Diego, CA
Medical Device Postmarketing Vigilance Reporting • March 18, 2010 • San Diego, CA
Adverse Events: Managing and Reporting for Medical Devices • March 18-19, 2010 • San Diego, CA
Drug Safety and Pharmacovigilance • March 18-19, 2010 • San Diego, CA
Regulatory Intelligence • March 19, 2010 • San Diego, CA
Advanced Clinical Research Coordinator • March 23, 2010 • Philadelphia, PA
Adverse Events: Managing and Reporting for Pharmaceuticals • March 23-24, 2010 • Philadelphia, PA
Clinical Trials for Pharmaceuticals: Design and Development • March 23-24, 2010 • Philadelphia, PA
Conducting Clinical Trials Under ICH GCP • March 23-24, 2010 • Philadelphia, PA
Conducting Clinical Trials in Emerging Regions • March 24-25, 2010 • Boston, MA
Patient Recruitment and Retention • March 25-26, 2010 • Philadelphia, PA
Clinical Drug Development • March 25-26, 2010 • Philadelphia, PA
Complete Live Listings
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