ClinPlus Data Management
The heart of the ClinPlus® Suite has been engineered to meet the strict requirements and high expectations of today's clinical data management professionals. ClinPlus Data Management includes all the tools required to design, run, and manage a clinical trial from start to finish, making it the most comprehensive, flexible, and resource-friendly clinical data management system on the market. Our latest version of ClinPlus Data Management supports 64-bit processing and has direct integration with ClinPlus Coding, offering you the most productive SAS-based data management and coding suite available. Find out more...
ClinPlus Clinical Trial Management (CTMS)
An extremely flexible and scalable web-based, .NET-based software solution that empowers pharmaceutical organizations, biotechnology organizations, madical device manufacturers and contract research organizations (CROs) to manage clinical trial operations more productively and efficiently. The system can be installed, hosted or delivered as a Software-as-a-Service subscription, making it very attractive for emerging organizations that might lack financial or human bandwith to set-up trials. Find out more
ClinPlus Coding
A very powerful, quick and flexible adverse event and medication coding tool that provides accuracy and consistency for all your needs. Client's have been able to cut their coding toime in half when using this tool, and it works to code SAS, SQL and Oracle data. ClinPlus® Coding also supports virtually any dictionary, including MedDRA, WHOdrug (B-1, B-2 and C formats), COSTART, WHOart, ICD9, ICD10 as well as custom dictionaries and multiple versions of the same dictionary. Find Out More...
ClinPlus Report
Our powerful tables and listings workhorse used by most Tier 1 Pharma biostats groups has the versatility to produce complex statistical summary tables and simple data listings quickly and easily from all types of clinical data. New enhancements include a SDTM to ADaM data conversion tool as well as an extensive template library which permit cloning and rapid T&L authoring and branding of new templates. Clients report up to an 80% reduction in program development time. Find Out More...
CTMS
ClinPlus offers their software solutions for clinical trial applications including their Clinical Trial Management (CTMS) to provide pharmaceutical organizations, biotechnology organizations, medical device manufacturers and contract research organizations. This system can be installed, hosted or delivered as a Software-as-a-service subscription to make it an even more attractive option for emerging organizations lacking the financial or human bandwidth to set up trials. ClinPlus offers an entire suite of clinical trial products and services that meet the strict requirements and high expectations of today’s clinical data management professionals.
ClinPlus Data Management includes all of the tools you need to design, run, and manage a clinical trial from start to finish. The latest version supports 64-bit processing and has direct integration with ClinPlus Coding so you get the most productive SAS-based data management and coding suite available. CTMS software is effective where other software has failed. CTMS has proven to be intuitive and straightforward enough to achieve rapid deployment and training across an organization so that it frequently leads to a reduction in time-to-market.
The trial management software provides you with a .NET software solution that will empower your organization to manage and collaborate on clinical trial operations and expedite clinical trial design and study set-up more productively and efficiently. You benefit from a secure, stable and centralized access to multiple sites, trials, and programs. You can efficiently collect and manage patient and trial administration data and dramatically reduce trial administration costs.
ClinPlus Coding is a part of the clinical trial suite that offers powerful, quick and flexible adverse event and medication coding to ensure your coding is accurate and consistent. ClinPlus Coding has allowed clients to cut their coding time in half when they used this tool to code SAS, SQL, and Oracle data. It also supports virtually any dictionary, including MedDRA, WHOdrug (B-1, B-2 and C formats), COSTART, WHOart, ICD9, ICD10 and custom dictionaries and multiple versions of the same dictionary.
ClinPlus Report offers versatility to produce complex statistical summary tables and simple data listings quickly and easily from all types of clinical data. The software is made with new enhancements including a SDTM and rapid T&L authoring and branding of new templates. Like other clients, you may experience up to an 80% reduction in program development time.
To request a demo of the CTMS software or ask a question about any of the products that make up the ClinPlus Suite, call 1-866-ClinPlus. You can also learn more about the products and services available at www.clinplus.com. ClinPlus offers outstanding services that will help you manage your clinical trials easily and with the features you need specifically for your situation. Save money while enjoying a better way of tracking and comparing data. Their software solutions are based on many years of research to provide you with the optimum product that will help you broaden your trial horizons. Give them a trial run and you will see that their solutions are extremely flexible and allow you to define your unique standards and requirements for clinical studies. Meet all of your demands from multiple-study sponsors while you satisfy the strict guidance requirements of the FDA, EMEA and other regulatory authorities worldwide!
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