March 20, 2010
| Bio-IT World > Featured Events
Featured Events

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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

Attend the 2010 BIO International Convention in Chicago 

Don’t wait! Now is the time to register for The Global Event for Biotechnology. May 3-6, 2010, at Chicago’s McCormick Place. Join more than 15,000 colleagues and industry leaders from around the world for strategic discussions on latest trends.

Have a presence at exclusive one-on-one partnering meetings and take advantage of special networking opportunities. This is the place to access the innovations, resources and collaborations you need to strengthen your business for tomorrow and help biotech fulfill the promise to Heal, Fuel, Feed The World®. Visit convention.bio.org to search events, sessions and exhibitors

 

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

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

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

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 

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
 

To have your event featured here, contact  Lynn Cloonan for more information.

 

White Papers & Special Reports

oracle_clinical
eClinical Visions - Clinical Trial Management: Enabling Operational Efficiency
Sponsored by Oracle

Read how contributors from Genzyme, Duke Clinical Research Institute, Accenture, Oracle Health Sciences and others address some of the most pertinent challenges facing the biopharmaceutical industry including... Globalization of clinical trials driven by the need to reduce costs and recruit participants; greater outsourcing; escalating regulatory demands; increased trial complexity; and post-marketing studies. Download this paper to gain new insight into:

  • Recent progress made in addressing these challenges
  • Expert opinion on clinical trial management systems (CTMS) for improving trial efficiencies
  • How to cut trial costs and enhance the productivity of trial participants


oracle_RDC
Remote Data Capture – Acquisition and Analysis
Sponsored by Oracle

Today nearly half of all clinical trials are conducted electronically, and rising! Electronic Data Capture (EDC) technology provides industry-wide opportunities, along with challenges, that are being addressed. In this informative report industry experts and users from Pfizer, PPD, C3i and Oracle Health Sciences discuss the impact of EDC and its newest zero footprint; online iteration.  It can used anywhere, world-wide, where the Internet is available while placing greater onus on global trial support. The critical focus of this new technology is that it must support the work of the person at the heart of the clinical trial system– the investigator. Download this report to learn more about:

  • Trends and Issues in an Electronic Clinical Data Management World
  • The New Remote Data Capture Paradigm 
  • Improving and Monitoring Clinical Data Management in the eClinical Age
  • Optimizing and Supporting Remote Data Capture


oracle_video
Technology Video Report: A Day in the Life with Remote Data Capture (Next-Gen EDC)
Sponsored by Oracle
See why Oracle Remote Data Capture (RDC) Onsite is the next generation in electronic data capture with its user-friendly method to collect, clean, review, and verify clinical trial data. Providing unprecedented performance with real-time data capture, Oracle RDC Onsite simplifies source data verification. With a clear, consistent view of study data across all sites, the benefits include reduced monitoring time, decreased queries and discrepancies, and less time to database lock.



Life Science Webcasts & Podcasts

Predict or Perish! Shaping the Practices of Clinical Trials
Decisionview webinarSponsored by:  DecisionView

Predictive Analytics are a key differentiator in running your clinical trials successfully through 2010 and beyond. They will help you to optimize your patient enrollment, reduce your clinical operations costs and minimize your financial liability in the clinical supply chain. In this session, you will:
• Learn what predictive analytics are and what they are not
• Understand why you need predictive analytics to run your clinical trials, and
• Explore how predictive analytics will shape the future of clinical trials

Download Now. 

 



More Podcasts

Job Openings

The University of Washington Department of Genome Sciences is seeking a LINUX SYSTEMS ENGINEERING MANAGER to lead a team in a diverse scientific computing environment that includes multiple HPC systems, petascale storage, and custom application servers. Apply online at UW Hires for req number 61505.  http://www.washington.edu/admin/hr/jobs/

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