ClinPlus® Coding Earns UMC Certification

July 15, 2012

New York, NY/Bound Brook, NJ – June 15, 2012 DZS Software Solutions (DZS), a provider of software products that support several aspects in the performance of clinical trials, today announced achievement of certification by the Uppsala Monitoring Centre (UMC) for their ClinPlus Coding product.  The UMC Certification Program ensures that software vendors are providing tools that will give users full value and benefit of their WHO Drug Dictionary subscription.  The WHO Drug Dictionaries are the world’s most comprehensive source of medicinal product information. They are used by pharmaceutical companies, clinical research organizations and drug regulatory authorities to identify drug names, active ingredients and therapeutic use, in the course of clinical trials and drug safety surveillance.

The current version of ClinPlus Coding was engineered for optimal performance with the WHO Drug Enhanced Dictionary with certification as a goal.  The ClinPlus Coding software has past all test cases in the rigorous certification process demonstrating the ability to take full advantage of the ever evolving WHO Drug Dictionaries.  The UMC certification also provides software developers with free training and a software development kit, including documentation and examples

“We were very impressed with the ClinPlus Coding system’s performance and features as the system was being put through the rigorous certification process.  This system clearly demonstrated an excellent ability to work with the WHO Drug dictionaries in an efficient and intuitive manner.”  – Ola Strandberg, Vendor Liaison Officer

“Though this certification is certainly significant for us, it is more important to our customers in that they can be confident that the coding software they rely on works in harmony with the dictionaries they use”, said Greg Wagner, ClinPlus Coding Product Manager at DZS.

More information about the Software Certification Program is available at

About the Uppsala Monitoring Centre

The Uppsala Monitoring Centre (UMC) provides tools and resources to enhance clinical trials and drug safety operations, ranging from international monitoring of drug safety data to lexicon products and advanced tools for data analysis. Our main products are:

• The WHO Drug Dictionary Enhanced is the world’s most comprehensive dictionary of medicinal product information and de-facto standard for coding concomitant medication in clinical trials and adverse event reporting.

• VigiBase™ – the WHO adverse drug reaction database, which is the world’s largest and most comprehensive resource of international drug safety data.

As a centre of scientific excellence, UMC has extensive experience of database administration and data mining complex sets of clinical data. To advance this work, UMC has developed a range of products and techniques for companies and organizations working with life sciences.

About DZS Software Solutions, Inc.

DZS Software Solutions, Inc. is a privately held company founded in 1996 providing clinical trials software for clinical data management and analysis to the biotech and pharmaceutical industry worldwide. Over 60 clients globally presently use ClinPlus® software for data collection and capture, data cleansing, coding, analysis, clinical trial management and reporting. When the software is coupled with DZS services and training, many ClinPlus clients have dramatically improved productivity and maximized the value of clinical research investments and gained a competitive advantage to get medicines and products to market faster.

The ClinPlus® Software 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.

The ClinPlus® Software Solutions Suite’s unmatched cost-of-entry, scalability, flexible delivery options and exceptional training and support have gained DZS a reputation for delivering exacting quality and helping clients achieve early visibility to reliable clinical data. DZS software engineers possess decades of statistical analysis, clinical data management, clinical project management, and ADE/Drug coding and table/list/report building experience. This real-world experience is incorporated into every ClinPlus® system design and is evident in the reliability and enhanced features found in every system!