Order CD  Missed the event? While we can't make up for missed networking opportunities, we can offer you all the speaker's slides & research papers our delegates received on-site on CD. Stay abreast of clinical trial operation issues related to Clinical Trial Optimization, Forecasting, Feasibility, Site Selection, Recruitment, Data Collection, Managing Post-Marketing Studies and Alliances, as well as issues related to the Sunshine Act. Each program of SCOPE 2013 featured presentations and discussions offering different views and perspectives on poignant issues that the field currently faces. Contact information for all our speakers, sponsors, exhibitors, and media partners are included.  



  2013 SC2 Cover ThumbNEW! Clinical Trial Monitoring and Compliance: The Role of the CRA in Supporting Subject Recruitment and Successful Study Conduct
February 4, 2013
In this DVD, we will discuss the ever-changing role of the CRA and explore ways in which this relationship can be leveraged to maximize productivity with study sites. 
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   2013 SC3 Cover ThumbNEW! Understanding and Implementation of the Affordable Care Act and Sunshine Act on Clinical Trial Management
February 4, 2013
In this DVD, we will discuss the new "sunshine provisions" in the Patient Protection and Affordable Health Care Act ("PPACA") and its implications and effects on clinical trial operations. 
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   2012 DVD CoverEMR/EHRs: Utilization of Electronic Health Record Data For Clinical Research
February 6, 2012
In this DVD, we will discuss the potential benefits and risks involved in mining information outside of controlled trials to create insights on diseases, drugs, and patient populations and to optimize the conduct of clinical trials. 
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  Designing and Implementing a Clinical Enrollment Plan
March 8, 2010
CHI's Third Annual "Patient Recruitment in Clinical Trials: Strategically Planning a Successful Recruitment and Retention Program" was held March 8-9, 2010 at the Crowne Plaza Philadelphia City Center in Philadelphia, PA. Patient recruitment and retention are critical to drug development programs. Patient recruitment if not adequately planned for can extend your development timeline by a number of years. Retention of patients throughout the life of a clinical trial is essential in order have complete data sets for your analysis and subsequent filings. In order to optimize both you have to have a plan. This conference is intended to cover the topics one should consider when drafting and strategically implementing a patient recruitment and retention plan for a clinical development program. 
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  eCTD 2010: Achieving Efficiency and Compliance in Electronic Submissions
March 8, 2010
CHI's Inaugural "eCTD 2010: Achieving Efficiency and Compliance in Electronic Submissions" was held March 10, 2010 at the Crowne Plaza Philadelphia City Center in Philadelphia, PA. Filing new submissions is time consuming and costly to both regulators and drug development organizations. Global regulatory agencies are committed to improving the approval process and the electronic Common Technical Document (eCTD) is seen as a practical solution. It has been mandated in some countries and, to date, over 30,000 eCTD sequences have been submitted to the FDA alone. Despite the promise of eCTD to move your data through the approval process more efficiently, there are challenges to adoption and implementation. This course will discuss how to achieve efficiency and compliance in electronic submissions. Click here for more information



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In Memory of Gerald “Jerry” Matczak
Matczak Jerry

Gerald “Jerry” Matczak, lead consultant in clinical innovation at Eli Lilly & Co., was a rare breed in the pharmaceutical world, someone who not only embraced social media, but also listened to activist patients. He has been a part of the SCOPE conference since its inception and won the Patient Engagement Award on Wednesday, the day before his passing. Matczak died suddenly on Feb. 2 at age 54. We will all miss him.

– Cambridge Healthtech Institute (CHI)