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Outsourced Services and Staffing from DZS Clinical Services

Developing an effective team for clinical trial work is a difficult and ongoing process, and delays in final production or data output are common. Statistics show that an overwhelming number of clinical trials fail to meet the initial deadlines set by management, and that as many as 95 percent of all clinical trials over the last decade have resulted in final production or data output delays of a month or more. The costs associated with continuing a trial for a month can easily stretch a budget to the breaking point, resulting in lost talent; incomplete, fudged, or inaccurate data; or even a scrapped clinical project. An effective data management outsourcing solution can prevent such problems.

  • DZS Clinical Services streamlines your workflow, eliminating any potential logistical or software related slowdowns. Using ClinPlus data management and coding software is both robust and organic, providing all the power and versatility of any competing unified software system and a completely stable back-end database module, but with a flexibility that allows you to produce and work within your own specified workflow and customized coding library.
  • At DZS Clinical Services, Inc., we understand that implementing a data management outsourcing solution is a popular way to keep costs down and workflow up, and our software interface is designed to support a broad range of users who have widely diverging experience in a number of different software systems. Our user interface was created to provide a “best of all possible worlds” approach to navigation and data entry, minimizing required training time and accelerating the familiarization process for nearly all users. Since clinical data management outsourcing often requires the employment of individuals who are far removed from the center—sometimes even in other countries—the robust design and all-encompassing interface of ClinPlus data management will make consolidating talented resources within a single operating system so much easier than contending with outsourcers who may be using data management systems of varied origin.
  • From the beginning, DZS and ClinPlus software were built to support clinical data-management outsourcing, and the flexibility of our systems allows you to craft a custom workflow and proprietary coding library specific to the needs of your organization. Since outsourcing data management is becoming increasingly common, we are continually upgrading our software framework in order to further simplify the translation work required for data-management outsourcing tasks.
  • It should be noted that all ClinPlus software products are designed to provide real-world answers to the increasingly complex challenges of research and development, trial administration, data management, coding and reporting in the pharmaceutical and medical community. ClinPlus is the end product of years of research that has been aimed at determining the best way to combine multiple disciplines, including coding services, statistical programming, clinical data-management outsourcing, SAS consulting, and CDISC/SDTM/ADaM data conversion. We are very familiar with the supplier selection process in the pharmaceutical, medical device, and biotech industries, and we’ve spared no expense to ensure that DZS Clinical Services and the ClinPlus systems provide all the proper tools you need to properly manage every aspect of your clinical trial, from start to finish.
  • Regardless of the needs of your organization or the level of data management outsourcing your project requires, DZS and ClinPlus provide the flexibility and power you need to ensure that your project runs smoothly and efficiently.

CLINICAL TRIALS

The State of Clinical Trials 2012

Most clinical trials currently do not meet their deadlines and approximately 85% experience delays; 95% of these must contend with delays of more than a month. As a result, the drug development business model has been modified considerably to include clinical data management outsourcing solutions to help overcome these delays.

In addition, Pharmaceutical, Biotechnology, and Medical Device organizations are increasingly seeking unique expertise and capabilities when selecting sourcing partners -- ones with functional services like data management, coding, biostatistics and statistical programming, and laboratory facilities, logistics and translation services all gaining significant importance.

Post-marketing studies have also seen an increase in recent years, owing to the importance given by the medical community to the long-term safety aspects of drugs. Technical know-how, capacities, compliance and the ability to complete clinical trials within the stipulated time are the primary factors that companies examine before making a decision.

At DZS Clinical Services, we realize that selecting the right strategic outsourcing partner is important. We are very familiar with the rigorous supplier-selection process used by many of our CRO, Pharmaceutical and Biotech and Medical Device clients, especially when they are evaluating suppliers in technology markets.

DZS Clinical Services is designed specifically keeping in mind the growing challenges of pharmaceutical companies in the year 2012 in the areas of research and development and trial management. Our services focus on outsourcing of high-end niche transactional processes, such as SAS consulting and statistical programming, clinical data management, medical coding, study set-up, clinical trial project management and CDISC/SDTM/ADaM data conversion. 

Contact Us

"I have received excellent support from the ClinPlus staff. They have answered all our questions, resolved any issues we have had or given us timelines for those that could not be resolved immediately."

Jennifer Dugan

Manager of Clinical Data Management - Allied Research International

Contact DZS Today! Contact DZS Today!


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