Research & Development: Page 101


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    Table of Contents

    Table of Contents Letter from the Editor Forum on Marketing Modern Marketing in the Making: Marketing executives from pharmaceutical, biotechnology, device, and diagnostic companies, ranging in size from small specialty to midtier to large and global, share common challeng...

    By PharmaVoice Team • Jan. 2, 2008
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    On the Calendar

    Industry Events October 15-16, 2003, Wardman Park Marriott Hotel — Washington, D.C. eSubmissions for Global Compliance This Marcus Evans conference will focus on electronic document management and publishing. Key topics will include an ICH update, changes in eCTD specifications, CDISC data standa...

    By PharmaVoice Team • Jan. 2, 2008
  • Trendline

    Artificial intelligence & machine learning

    After years of excited buzz around the potential of artificial intelligence and machine learning, pharma has begun to realize the true implications and potential value of these technologies.

    By PharmaVoice staff
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    PharmaCounsel

    The Effects of the HIPAA Privacy Policy Rule on Clinical Research and Registries On April 14, 2003, the privacy rule took effect and most covered entities must now comply with its provisions. The rule establishes minimum federal standards for safeguarding the privacy of individually identifiable ...

    By PharmaVoice Team • Jan. 2, 2008
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    E-Media

    Dendrite Launches Sample Program Dendrite International Inc. has launched its One-Source Sample program, which serves the entire life cycle of sample-product promotion and blends market-leading software applications with best-in-class consulting and professional services. Helping to ensure compli...

    By PharmaVoice Team • Jan. 2, 2008
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    E-Clinical Services: The Evolving Role of the Technology Vendor

    The E-Arena etrials Worldwide Inc. With the extensive e-clinical options available to trial sponsors, as well as the continued advancement of technology, there is no question that careful consideration must be given to what tools to employ in clinical-trial research. But choosing a solution d...

    By PharmaVoice Team • Jan. 2, 2008
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    Site Qualification and Training: Immediate Time, Cost, and Performance Improvements

    ePharmaLearning Inc. ePharmaLearning Inc., Conshohocken, Pa., is an industry leading site qualification, clinical e-learning, and site activation company. For more information, visit epharmalearning.com. The keys to improving a clinical trial’s operational success include selecting the b...

    By PharmaVoice Team • Jan. 2, 2008
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    Timely Enrollment and Retention: Keys to a Successful Clinical Trial

    Ultimately, trial enrollment will always require extensive human interaction between all interested parties. Tools that can facilitate the magic that occurs when new methods of treatment get to market can change lives. Key to a successful clinical trial is timely enrollm...

    By PharmaVoice Team • Jan. 2, 2008
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    Clinical Teams Say Sites Can Do Recruitment, But Can They?

    Clinical Teams Say Sites Can Do Recruitment, But Can They? Why a fixed budget for every site sets up a study for failure. Patient Recruitment The best strategy is to customize recruitment campaigns to ensure that recruitment is timely and cost-effective. El...

    By PharmaVoice Team • Jan. 2, 2008
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    Five Steps to Successful Electronic Data Management Vendor Selection

    While the pharmaceutical industry has been working to adopt e-clinical technology for more than a decade, almost 70% of e-clinical technology implementations fail to meet expectations. Why the lack of success? There are countless reasons, but one of the most important is the complexity surroundin...

    By PharmaVoice Team • Jan. 2, 2008
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    Investigator Initiated Trials: The 800-Pound Gorilla

    The Clinical-Trial Process Investigator initiated trials (IITs) can be a significant boon to a company with a new drug or device or sometimes even an older product. Why? Because physicians are engaging in something they truly want to do (it’s their idea, after all), at a cost that’s generally ...

    By PharmaVoice Team • Jan. 2, 2008
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    Improving Clinical-Trial Performance

    The Clinical-Trial Process Improving Clinical-Trial Performance Effectively managing the vast number of dispersed resources involved in conducting a clinical trial requires a cohesive approach that assures clinical study and regulatory knowledge to achieve hig...

    By PharmaVoice Team • Jan. 2, 2008
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    Clinical Document Development: Planning for Accelerated Timelines

    Jean Hosutt, Ph.D., Director, Medical Regulatory Writing Clinical Document Development: Planning for Accelerated Timelines clinical document development Active planning is required to facilitate the partnership between the sponsor and medical-writing contractor resultin...

    By PharmaVoice Team • Jan. 2, 2008
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    Clinical Data Strategies for Performance Optimization

    Octagon Research Solutions Inc. Data Standards Organizations that hesitate to embrace these standards as opportunities will be at a competitive disadvantage. They will continue to struggle with the tactical “cost” of transforming the ...

    By PharmaVoice Team • Jan. 2, 2008
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    Letter from the Editor

    The Drug Information Association (DIA) will play host to the largest group of exhibitors and attendees in its 41-year history. More than 815 exhibit booths representing more than 550 companies will be in attendance at the Washington Convention Center in Washington, D.C., June 26-June 30, 2005, ...

    By PharmaVoice Team • Jan. 2, 2008
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    Table of Contents

    Letter from the Editor The Forum Clinical Services: Outsourcing: A Vital Clinical Strategy — A large, unmet need exists for improved research and development (R&D) productivity within pharmaceutical and biotechnology companies. Outsourcing discovery research, clinical trials, and f...

    By PharmaVoice Team • Jan. 2, 2008
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    The Phase IV Juggernaut: Best Practices for Success

    Dimensional HealthCare Inc. Late-stage success depends on an in-depth understanding of the Phase IV scientific drivers, the commercial objectives, and the integration of clinical and marketing knowledge. Adam Serody VP, Clinical Solutions The Phase IV Juggernaut: ...

    By PharmaVoice Team • Jan. 2, 2008
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    PharmaTrax

    CME Programs Accredited by Universities and Societies Receive Preference Continuing medical education (CME) programs created by medical communications agencies achieve a higher level of acceptance among physicians when they are accredited through partnerships with respected university medical sch...

    By PharmaVoice Team • Jan. 2, 2008
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    Translational Research: Making the Transition from R to D

    Translational Research: Making the Transition from R to D There is a growing interest in translational research, which aims to bridge the gap between advances in basic research and the development of safe and effective therapies. June 2005 PharmaVOICE Despite increased investment in research and ...

    By Denise Myshko • Jan. 2, 2008
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    Cover

    Clinical-Trial Transparency: The Pros and Cons Representing Biotech with David King DTC: The Next Evolution PharmaVOICE www.pharmavoice.com June 2005 Volume 5, Number 6 Download PDF

    By PharmaVoice Team • Jan. 2, 2008
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    Table of Contents

    on the cover The time for transparency The government, medical journal editors, and general public are clamoring for the pharmaceutical industry to provide complete information about ongoing and completed clinical trials. There has been a flurry of activity, announcements, and mandates in this ar...

    By PharmaVoice Team • Jan. 2, 2008
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    On the Calendar

    June 6-7 Pharmaceutical Marketers KnowledgeShare Forum 2005: Building Brand Differentiation in the Current Regulatory Climate Airport Marriott, Philadelphia This is a PharmaVOICE event, subscribers are eligible for a 15% discount; register using code PVMKS05. For more information, contact Micah L...

    By PharmaVoice Team • Jan. 2, 2008
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    E-Media

    New Electronic and Web-based Applications, Sites, and Technologies E-Media June 2005 PharmaVOICE SAS Upgrades Scientific Discovery Solutions In response to the need for modernization in the drug-development process, SAS Institute Inc. has made significant upgrades and additions to its Scientific ...

    By PharmaVoice Team • Jan. 2, 2008
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    What's New

    New Healthcare-related Products, Services, and Companies PMI Appoints Task Force to Oversee CME Compliance Pri-Med Institute (PMI) has named a task force of medical and educational experts to ensure that all of its continuing medical education (CME) programs meet and exceed the new Standards of C...

    By PharmaVoice Team • Jan. 2, 2008
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    What's on Your Mind -- Opinions

    Opinions What’s on your mind What have you heard lately? In the September issue of PharmaVOICE, we asked readers to relate the most surprising statistics or strange facts that they have come across. PharmaVOICE learned that every human spent about half an hour as a single cell and that 70% of con...

    By PharmaVoice Team • Jan. 2, 2008
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    Letter from the Editor

    Letter from the Editor By Taren Grom Editor Driving business forward According to the U.S. Small Business Administration, more than 50% of small businesses fail in the first year and 95% fail within the first five years. Some entrepreneurs describe their decision to set up their own business as a...

    By Taren Grom • Jan. 2, 2008