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About DZS

The ClinPlus Solutions Suite for Clinical Trials provides premium tools required by pharmaceutical companies, contract research organizations (CROs), biotechs and medical device manufacturers, to expedite clinical trials and meet the strict data-formatting requirements of the FDA and other global regulatory agencies.

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ClinPlus Report - Tier 1 Pharma authoring tool.

  
  
  
  

ClinPlus Report

ClinPlus Report is the industry's most widely-proven, SAS®-based, statistical table and listing authoring tool for creating the highest quality statistical tables and listings from any type of clinical data.

ClinPlus Report allows you to easily produce a variety of complex FDA-ready tables and listings in New Drug Application (NDA) quality. It also produces effective statistical tables, and utilizes over 70 different statistical values across numerous SAS/STAT procedures. You can choose precision, group and class variables, sub-setting, or subtotals, and you always have the final word in controlling the appearance of the table. ClinPlus Report's extensive format control features are a tremendous asset when preparing any summary you require and producing tables and listings in any format you need.

Reports generated with ClinPlus Report promise to be consistent, of superior quality and based on your standards, even across disparate programming groups. And you will benefit from the peace-of-mind that comes in knowing the reports you deliver are produced using a validated product and are totally CDISC-compliant when included in your eventual NDA, eCTD, NeeS marketing authorization applications.

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