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July 29, 2010
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Featured Events

6th Leveraging Healthcare Technology to Monitor & Improve Clinical Outcomes

Utilizing HIT Applications and Data to Optimize Efficiency and Increase Patient Safety

AUGUST 11-12, 2010, Hyatt at the Bellevue, PHILADELPHIA, PA

Formerly known as the Integrating Electronic Health Records and eClinical Technologies Conference, this year’s expanded topic scope reflects the industry’s interest beyond integration to the utility of the data collected by healthcare information technologies and the application of this data to monitor and improve clinical outcomes. Capitalizing on the increasing HIT data that is now available resulting from government led initiatives to increase EHR adoption, drug manufacturers, providers, hospitals, and many other stakeholders in the healthcare industry now need to learn what to do with this HIT technology and data to optimize efficiency and increase patient safety.

 

Personalized & Translational Medicine USA
September 20-21, 2010, Radisson Hotel Boston, MA

Companion diagnostics, personalized therapies, and cross industry partnerships set to dominate the next decade. This event is dedicated to fostering a meeting platform and cover all the aspects of this complex endeavor, with the ultimate goal of taking product development to the next level. Move from Blockbuster to Nichebuster to reach the right patients.

 

2010 Translational Research Excellence Conference (TRX10)
October 11-13 Brisbane Convention & Exhibition Centre Brisbane, Australia

TRX10 aims to set new standards for the region in stimulating trans-disciplinary collaborations across all areas of human disease research, drug and diagnostic discovery and development, IT and bioinformatics.  In order to create an international awareness focussed on the Asia-Pacific Region’s current translational biomedical research, IT and bioinformatics capabilities, TRX10 brings together these diverse yet related disciplines and stakeholders in the relaxed subtropical surroundings of Brisbane in Queensland, and provides a platform where delegates can share issues and best practices related to translational research, policy-making, enabling technologies and bioinformatics.

CHI Events

The Immunotherapeutics & Vaccine Summit • August 17-19, 2010 • Cambridge, MA

Novel Vaccines: Design & Development • August 17-18, 2010 • Cambridge, MA

Production & Manufacturing of Vaccines • August 17-18, 2010 • Cambridge, MA

Novel Vaccines: Adjuvants & Delivery Systems • August 18-19, 2010 • Cambridge, MA

Challenges in Preclinical Development • August 18-19, 2010 • Cambridge, MA

The Bioprocessing Summit • August 23-26, 2010 • Boston, MA

Optimizing Cell Culture Technology • August 23-24, 2010 • Boston, MA

Affinity Tag Protein Purification • August 23-24, 2010 • Boston, MA

Next Generation Dx Summit • August 24-26, 2010 • Washington, DC

Enabling Point-of-Care Diagnostics • August 24-25, 2010 • Washington, DC

Cancer Diagnostics • August 24-25, 2010 • Washington, DC

Co-Development of Drug and Diagnostics • August 25-26, 2010 • Washington, DC

Molecular Diagnostics for Infectious Disease • August 25-26, 2010 • Washington, DC

Optimizing Mammalian Cell Lines • August 25-26, 2010 • Boston, MA

Baculovirus Technology • August 25-26, 2010 • Boston, MA

ADAPT 2010: Accelerating Development & Advancing Personalized Therapy • September 13-16, 2010 • Arlington, VA

Personalized Medicine • September 14-16, 2010 • Arlington, VA

Translational Cancer Medicine • September 14-16, 2010 • Arlington, VA

Biomarker Development • September 14-16, 2010 • Arlington, VA

Adaptive Clinical Trials • September 14-16, 2010 • Arlington, VA

Diagnostic Development • September 14-16, 2010 • Arlington, VA

NGx: Evolution of Next-Generation Sequencing • September 27-29, 2010 • Providence, RI

Next-Generation Sequencing Data Management • September 27-29, 2010 • Providence, RI

Cloud Computing Training: Amazon Web Services (AWS) • September 30 - October 1, 2010 • Providence, RI

Accelerating Proof of Concept • October 4-6, 2010 • Philadelphia, PA

Clinical Training Forum • October 4-5, 2010 • Philadelphia, PA

Bio-IT World Europe • October 5-7, 2010 • Hannover Germany

IT Infrastructure & Informatics: Data Storage, Analysis and Visualization • October 5-6, 2010 • Hannover Germany

Next Generation Sequencing Data Management • October 5, 2010 • Hannover Germany

PEGS Europe • October 5-7, 2010 • Hannover Germany

Novel Antibody Constructs and Alternative Scaffolds • October 5-6, 2010 • Hannover Germany

Protein Expression and Cell Line Development • October 5-6, 2010 • Hannover Germany

Molecular Diagnostics Europe • October 5-7, 2010 • Hannover Germany

Moving Molecular Diagnostics from Bench to Bedside • October 5-6, 2010 • Hannover Germany

NGS: The Ultimate for Molecular Diagnostics • October 5-6, 2010 • Hannover Germany

Point-of-Care Diagnostics • October 6-7, 2010 • Hannover Germany

Empowered Bispecific Antibodies and Antibody-Drug Conjugates • October 6-7, 2010 • Hannover Germany

Difficult Protein Expression and Purification • October 6-7, 2010 • Hannover Germany

IT Infrastructure & Informatics: Collaborative Software, Standards, & Web Technologies • October 6-7, 2010 • Hannover Germany

Data Integration and Knowledge Management • October 6-7, 2010 • Hannover Germany

Fundamentals: Amazon Web Services for Science and Engineering • October 7-8, 2010 • Hannover-Laatzen Germany

China Pretrials 2010 • October 17-19, 2010 •

Immunogenicity Summit • October 19-21, 2010 • Philadelphia, PA





CHI Upcoming Short Courses

Single-Use Systems for Vaccine Manufacture • August 16, 2010 • Cambridge, MA

Vaccines Business Opportunities • August 16, 2010 • Cambridge, MA

Optimizing Media-Achieving Super Soup • August 23, 2010 • Boston, MA

Affinity Tag Purification Systems • August 23, 2010 • Boston, MA

Roadmap for Accelerating Commercialization of Molecular Diagnostics • August 23, 2010 • Washington, DC

Micro-and Nanofluidics in Diagnostics and Life Sciences • August 23, 2010 • Washington, DC

E. coli Innovations • August 24, 2010 • Boston, MA

Future of Point-of-Care Platforms • August 25, 2010 • Washington, DC

Executive ThinkTank: Drug-Diagnostic Co-Development • September 13, 2010 • Arlington, VA

Biomarker Assay Development and Validation • September 13, 2010 • Arlington, VA

NGS Data • September 26, 2010 • Providence, RI

Target Enrichment • September 26, 2010 • Providence, RI

Cloud Computing • September 28, 2010 • Providence, RI

Making Sense of Next-Gen Sequencing Data • October 4, 2010 • Hannover Germany

Cloud Computing for Life Sciences • October 4, 2010 • Hannover Germany

Visualization of Large-Scale Biological Data • October 4, 2010 • Hannover Germany

Micro-and Nanofluidics in Diagnostics and Life Sciences • October 4, 2010 • Hannover Germany

Protein Aggregation in Biopharmaceutical Products • October 4, 2010 • Hannover Germany

Management of Immunogenicity • October 4, 2010 • Hannover Germany

Technical Advice on Immunogenicty Assays • October 4, 2010 • Hannover Germany

Creating Synergy-Introduction to Biomedical Data Fusion • October 4, 2010 • Hannover Germany

Key Trends in Microfluidics • October 4, 2010 • Hannover Germany

Evidence Led Decision Making for Clinical Proof-of-Concepts • October 4, 2010 • Philadelphia, PA

Technical Advice on Assay Development, Validation and Sample Analysis • October 18, 2010 • Philadelphia, PA

Development of Cell-Based Neutralizing Antibody Assays • October 18, 2010 • Philadelphia, PA





Barnett Educational Services

Barnett Web Seminars

Trial Master File (TMF) for Sponsors: Set-Up and Maintenance • August 5, 2010 • Interactive Web Seminar

Final FDA Guidance: How to Complete the FDA Form 1572, Adequately & Accurately • August 5, 2010 • Interactive Web Seminar

10-Week CRA & CRC: Beginner Program • August 5, 2010 • Interactive Web Seminar

Adverse Event Monitoring for CRAs • August 6, 2010 • Interactive Web Seminar

Use of Notes to File in Clinical Trial Essential Documentation • August 6, 2010 • Interactive Web Seminar

Transitioning Pharmaceutical Professionals to Medical Device Professionals • August 10, 2010 • Interactive Web Seminar

Medical Device Reporting • August 11, 2010 • Interactive Web Seminar

Approaches to Address Challenges in Vendor Management • August 13, 2010 • Interactive Web Seminar

Corrective Action Plans • August 17, 2010 • Interactive Web Seminar

Investigator Initiated Trials: Roles and Responsibilities • August 17, 2010 • Interactive Web Seminar

Making Good Teams Better: Taking Your Cross-Functional Global Team to the Next Level • August 17, 2010 • Interactive Web Seminar

Medical Device Tracking • August 18, 2010 • Interactive Web Seminar

Key Components of a Successful Study Site Start-up, Management and Maintenance Strategy • August 19, 2010 • Interactive Web Seminar

Monitoring Reports: 10 Rules of Effective Report Writing • August 19, 2010 • Interactive Web Seminar

Adequate Sponsor Monitoring Systems In Anticipation of FDA Sponsor GCP Inspections • August 20, 2010 • Interactive Web Seminar

Introduction to Signal Detection and Data Mining • August 23, 2010 • Interactive Web Seminar

Good Clinical Practice: Practical Application and Implementation • August 24, 2010 • Interactive Web Seminar

Strategies for Managing Difficult Clinical Research Sites • August 24, 2010 • Interactive Web Seminar

FDA Proposed Rule 2010: Sponsor Requirements to Report Fraud • August 24, 2010 • Interactive Web Seminar

Conflicts of Interest in Clinical Research: Policy and Practice • August 25, 2010 • Interactive Web Seminar

Root Cause Analysis: Applying the Concept for Better Study Compliance • August 26, 2010 • Interactive Web Seminar

Sponsor Management of Investigator Non-Compliance • August 26, 2010 • Interactive Web Seminar

Auditing Clinical Research Studies • August 26, 2010 • Interactive Web Seminar

Fraud in Clinical Research • August 27, 2010 • Interactive Web Seminar

Principal Investigator Training: Roles and Responsibilities • August 27, 2010 • Interactive Web Seminar

Use of Notes to File in Clinical Trial Essential Documentation • August 27, 2010 • Interactive Web Seminar

Adequate Investigator Oversight: Gap Analysis Tool for Current Systems • August 31, 2010 • Interactive Web Seminar

Informed Consent Content & Process Requirements • August 31, 2010 • Interactive Web Seminar

Presentation Skills Training for Clinical Research Professionals • September 3, 2010 • Interactive Web Seminar

Final AE Regulatory Guidance • September 3, 2010 • Interactive Web Seminar

Source Documentation: What is Adequate & Accurate? • September 7, 2010 • Interactive Web Seminar

Pediatric Drug Development • September 8, 2010 • Interactive Web Seminar

10-Week CRA & CRC: Beginner Program (September 8 - November 10. 2010) • September 8, 2010 • Interactive Web Seminar

Introduction to Data Management • September 9, 2010 • Interactive Web Seminar

Trial Master File (TMF) for Research Sites: Set-Up and Maintenance • September 9, 2010 • Interactive Web Seminar

Special Considerations in Pediatric Trials for CRAs • September 10, 2010 • Interactive Web Seminar

Monitoring Reports: 10 Rules of Effective Report Writing • September 10, 2010 • Interactive Web Seminar

ABCs of Clinical Research for Clinical Administrative Support Staff • September 13, 2010 • Interactive Web Seminar

Essential Documentation in Clinical Trials at Research Sites • September 14, 2010 • Interactive Web Seminar

Monitoring Informed Consent: The Process and Document • September 14, 2010 • Interactive Web Seminar

Meeting International Safety Reporting Requirements • September 15, 2010 • Interactive Web Seminar



Barnett Live Seminars

Introduction to Clinical Project Management • August 9-10, 2010 • San Diego, CA

Preparing IND Submissions • August 16-17, 2010 • San Francisco, CA

CRA & CRC Beginner • August 16-18, 2010 • San Francisco, CA

FDA Meetings 101 • August 23, 2010 • Philadelphia, PA

Report Writing for CRAs • August 24, 2010 • Philadelphia, PA

Mastering Cost Management for Global Clinical Trials • September 7-8, 2010 • Boston, MA

Adverse Events: Managing and Reporting for Medical Devices • September 9-10, 2010 • Chicago, IL

Combination Products • September 9-10, 2010 • Chicago, IL

Working with CROs • September 9-10, 2010 • Boston, MA

Introduction to Clinical Project Management • September 9-10, 2010 • Boston, MA

Signal Detection and Case Processing • September 10, 2010 • Boston, MA

Gap Analysis • September 13, 2010 • Philadelphia, PA

Query Creation & Processing • September 13, 2010 • Philadelphia, PA

Comprehensive CRC Training • September 13-14, 2010 • Philadelphia, PA

Medical Device GCP Overview • September 13-14, 2010 • Philadelphia, PA

Adverse Events: Managing and Reporting for Pharmaceuticals • September 14-15, 2010 • Chicago, IL

Comprehensive Monitoring for Medical Devices • September 15-17, 2010 • Philadelphia, PA

Monitoring Clinical Drug Studies: Beginner • September 15-17, 2010 • Philadelphia, PA

Advanced GCP • September 20-21, 2010 • San Diego, CA

Clinical Project Management Advanced • September 20-21, 2010 • San Diego, CA

Medical Device Approval Process • September 20-21, 2010 • San Diego, CA

Query Creation & Processing • September 24, 2010 • San Diego, CA

Regulatory Intelligence • September 24, 2010 • San Diego, CA

Auditing Techniques for Clinical Research • September 27-28, 2010 • San Diego, CA

Drug Safety and Pharmacovigilance • September 27-28, 2010 • San Diego, CA

Patient Recruitment and Retention • September 27-28, 2010 • San Diego, CA

Developing Clinical Study Budgets • October 1, 2010 • Philadelphia, PA

Source Documentation • October 1, 2010 • Philadelphia, PA

Clinical Drug Development • October 4-5, 2010 • Philadelphia, PA

Clinical Trials for Pharmaceuticals: Design and Development • October 4-5, 2010 • Philadelphia, PA

The CRA Manager • October 4-5, 2010 • Philadelphia, PA

Data Management in the Electronic Data Capture Arena • October 11-12, 2010 • Philadelphia, PA

Advanced GCP • October 11-12, 2010 • Philadelphia, PA

Conducting Clinical Trials Under ICH GCP • October 11-12, 2010 • Philadelphia, PA

Comprehensive Monitoring for Medical Devices • October 13-15, 2010 • Chicago, IL

Drug Approval Process • October 14-15, 2010 • Philadelphia, PA

Monitoring Clinical Drug Studies: Advanced • October 14-15, 2010 • Philadelphia, PA

Clinical Project Management: Intermediate • October 18-19, 2010 • Boston, MA

Drug Development & FDA Regulations • October 18-19, 2010 • Chicago, IL

Clinical Trials for Medical Devices: Design & Development • October 18, 2010 • Chicago, IL

Pharmacokinetics • October 18-19, 2010 • Philadelphia, PA

Pharmacovigilance • October 18, 2010 • Philadelphia, PA

Preparing IND Submissions • October 18-19, 2010 • Philadelphia, PA

Statistical Concepts for Non-Statisticians • October 18-19, 2010 • Philadelphia, PA

Fraud in Clinical Research • October 21, 2010 • San Diego, CA

Global GCP Monitoring • October 21-22, 2010 • San Diego, CA

Monitoring Clinical Drug Studies: Beginner • October 25-27, 2010 • San Diego, CA

Working with CROs • October 25-26, 2010 • San Francisco, CA

Managing and Conducting Global Clinical Trials • October 25-26, 2010 • San Francisco, CA

FDA Meetings 101 • October 25, 2010 • San Diego, CA

Pharmacovigilance Audit • October 26, 2010 • San Francisco, CA


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



White Papers & Special Reports

oracle20723
The Role of Analytics in Transforming Healthcare
Sponsored by Oracle

Sharing many of the data challenges and opportunities faced by Healthcare, the Life Sciences industry remains focused on delivering new, innovative therapies and solutions to patients in a cost effective, timely and safe way. With spiraling R&D costs, new methods such as adaptive trials, and never ending need for deep pharmacovigilance, the Life Sciences companies that effectively use analytics to explore, monitor and optimize their business will rapidly become the new leaders.

Oracle’s strategy—built upon Enterprise Health Analytics and Health Data Warehouse Foundation—provides a powerful, practical, and extensible approach to delivering the IT analytics infrastructure required to confront the worldwide healthcare challenge.

Download Now


pegasystems
BPM-Based Case Management Approach to Optimizing Clinical Trial Efficiency
Sponsored by Pegasystems

Business Process Management (BPM) software offers liberation in the planning and management of clinical trials today. SmartBPM provides the components for automating critical clinical trial processes ranging from protocol development and patient enrollment to site management and investigator payments. Advantages are:

  • Potentially stunning return on investment at multiple levels.
  • A 500%, or better, increase in application development time by directly executing business requirements
  • Improved customer retention
  • A 50% possible reduction in training time

Discovered is opportunity to enhance relationships with investigators, subjects, and regulators while bringing momentum to a technology-impaired study startup phase. Learn more about SmartBPM in this complimentary white paper.

Download Now


Cmed paper
Next-gen Cloud-based eClinical
Sponsored by Cmed Technology

New technologies are available to leverage Cloud Computing in  managing clinical trial data. This paper discusses a next generation eClinical
platform that:

  • Speeds trial set up
  • Accommodates changes with zero downtime
  • Integrates effectively with other clinical trial technology systems

It is offered with either software-as-a-service (SaaS), or turnkey infrastructure options in which the user organization operates their own cloud using their IT teams, within their data centers. Read this paper to learn and decide how best to leverage cloud computing’s many strengths for your organization’s  particular needs.

Download Now
More White Papers & Special Reports
Job Openings

mskc logo
Software Engineer – Computational Biology Center

Memorial Sloan-Kettering Cancer Center seeks an Engineer to design and develop complex data analysis systems in support of cancer genomics research projects at the Computational Biology Center. Qualified candidate will have a BA, 5+ years of software development experience and expert knowledge of Java, SQL, and HTML.

Apply: www.mskcciscareers.org.  Equal opportunity and affirmative action employer.


Web Symposia
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Bio-IT World proudly presents the Bio-IT World Web Symposia Series covering a broad array of topics within the life sciences and drug development enterprise.

Leveraging BPM to Increase Efficiencies in Clinical Trial Case Management
August 3, 2010 | 1:00 – 2:30 p.m. EST
Sponsored by: Pegasystems
Program Details | Register Here 

 
Related Resources & Products
DVD Adverse Events for Medical Devices
Adverse Events: Managing and Reporting for Medical Devices

CRA Training Series (7 Volume Set) (2000)

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(717) 505-9701 ext. 125, or via email to Ashley.Zander@theYGSgroup.com.

Cambridge Healthtech Institute

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