Clinical Study Set-Up Services

Do you need help setting up a study and getting results fast? 

Our team of professionals has the industry knowledge and expertise to immediately increase your team’s productivity and expedite study set-up. We offer a standard set of services that includes database design, initial screen design and edit check programming. We can also offer clinical trial software and can configure services to meet any budget and timeline. We make sure that you get the results you need, when you need them!

We can integrate ClinPlus technology into your existing environment, in addition to providing you with customized study set-up and start-up services with a variety of training options for ClinPlus Data Management and ClinPlus Coding, ClinPlus Report and ClinPlus CTMS.

FLEXIBLE & FEATURE-RICH CLINICAL TRIAL SOFTWARE

The ClinPlus Data Management that is a part of the study set-up services is believed to be the most feature-rich, flexible and intuitive CDMS system ever marketed. The latest version of our clinical trial software has many additional features, including support for 64-bit architecture, to dramatically increase speed and performance. The software now integrates directly with the ClinPlus Coding 3.1 software to make you even more productive. Since ClinPlus has purposely retained the ease-of-use and low IT support requirements that clients have come to expect from ClinPlus, it is even easier to use than the original system.

CPDM can support paper-based and electronic studies, site-based entry, or any combination of the two within the same study. This system allows you to manage all of your clinical data within a single system, to ensure a smooth progression from entry of the first casebook, to a clean and secure database lock. CPDM is flexible enough to build complex data entry systems, as well as simple ones.

CODING: ACHIEVING CLEAN DATA

ClinPlus Coding is another valuable tool that resolves the challenges in achieving clean data throughout any study. Since the majority of data is collected at different sites by different physicians, as well as in different time zones and cultures, inconsistencies and variations in entered data are common. DZS/ClinPlus has developed Coding to be a flexible clinical coding solution in the industry that will meet all of your adverse events and drug coding needs.

CLINPLUS REPORT: CREATING ACCURATE TABLES

ClinPlus Report is a SAS-based system that is ideal for authoring safety and efficacy tables and listings, in addition to other tables and listings that include patient profiles. The report template library contains more than 60+ commonly used tables and can significantly increase programmer productivity when developing custom tables. Create simple data listings or complex statistical summary tables, while controlling the look and feel of how data and tables are formatted.

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