EDC/Data Management White Papers & Case Studies
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Grant Payment Practices: Five Requirements For Stronger Investigator Relationships
9/27/2012
In the clinical trials industry, profitability and regulatory compliance pressures continue to mount. Consequently, pharmaceutical companies are striving to maximize their research and development spending by reducing clinical trial cycle times and focusing on their core competencies—all while maintaining high standards of quality. By James M. Dicesare and Kevin T.Williams, Clinical Financial Services, LLC (CFS).
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Getting Data Protection Management Right
9/14/2012
Security policies and procedures must be in place to manage activities, both online and offline, for every individual within the chain-of-trust. According to a 2009 Ponemon Institute survey revealed that 59% of ex-employees admitted to stealing confidential company information, which is why enterprises today need to have a keen eye on human resources – the people within the chain-of-trust and the critical information assets that they create, manage, or otherwise have access to.
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Clinical Trials Business And Financial Management Services Brochure
9/5/2012
CFS Clinical is the only company to offer turnkey business and financial management services for clinical trials. We help CROs, biopharmaceutical sponsors, and medical device companies to address today’s complex management challenges.
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Contract & Regulatory Services Brochure
8/29/2012
With tight timelines and complicated regulatory documentation requirements, getting a clinical trial up and running quickly is easier said than done. Key milestones—including drug shipment, IRB approval, and patient randomization—can be achieved only after the successful negotiation of clinical trial agreements and completion of essential regulatory documents.
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Global Payment Services Brochure
8/29/2012
Biopharmaceutical and medical device companies rely on investigative sites to complete their clinical trials. Building strong relationships with high-quality sites is critical to addressing a number of key challenges – from the growing number of trials to mounting pressures to minimize cycle times. Yet investigative sites increasingly denounce unrealistic payment schedules and inefficient payment processes as not only frustrating but also threatening to their financial viability.
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Understanding ROI Using eSource Data In Clinical Trials
7/17/2012
Many clinical trial teams are tiptoeing into the world of eSource, anxious to reap the benefits, yet uneasy about the impact. To many, the unknowns seem daunting and overwhelming, and perhaps not worth the effort. To those who have taken the plunge, the value to the study team has far outweighed the initial investments.
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Lab Study Manager Brochure
5/9/2012
Endign is in the business of providing proven solutions to Pharma’s hardest software issues. Our Lab Study Manager package is no different, providing robust tracking of study timelines, financial aspects and proactive alerting.
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PiKo® Monitors Brochure
4/27/2012
Ideal for clinical trials, PiKo® Lung Health Monitors deliver lung function measurements not traditionally available through home monitoring.
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DSG Clinical Trials Products And Software Solutions
12/5/2011
Since our founding, DSG has transformed clinical trial data collection and analysis with its integrated suite of EDC software solutions. Below is a wide range of clinical trials software and services that we offer to our clients.
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The Economic Impact Of Using Target eClinical Trial Record (Target e*CTR®) In An 80-Center Study In Ulcerative Colitis
10/7/2011
Target Health Inc., a full service eCRO, has developed Target e*Clinical Trial Record (Target e*CTR®; patent pending), a web-based system that generates an electronic clinical trial source patient record without the need to collect patient information using paper records. There are clear advantages to the clinical sites not to have to maintain paper source records and not to have to transcribe paper records to EDC without the need to have an electronic medical record (EMR) or to have to integrate their EMR with EDC systems. There is also clear that if the clinical site can perform direct data entry (DDE)