Posted on Thu, Jun 10, 2010
DZS Software Solutions Inc. will unveil new functionality for their suite of clinical trial software products -Data Management, Coding, Report and Clinical Trial Management. Stop By Booth# 927
Bound Brook, NJ - June10, 2010 - DZS Software Solutions, Inc. plans on demonstrating several new enhancements for their clinical solutions at the upcoming DIA Annual Conference in Washington DC, June 13th-16th. (DZS is at Booth #927).
Since 1996, DZS Software Solutions Inc., innovators of the ClinPlus brand of products has been committed to providing the most technologically advanced clinical software products to manage the data of clinical trials, to life science professionals, helping them streamline the clinical trial process and accelerate the process of bringing life-enhancing medicines, biologics and devices to market.
Most recently, DZS responded to industry challenges to increase clinical trial productivity and reduce operating expense by launching a web-based clinical trial management system (CTMS) at last year's DIA Annual in San Diego. Since that time, the system has gained increasing acceptance because of its ability to improve site productivity, eliminate redundant systems and existing manual tasks and help enforce adherence to trial procedures and regulatory compliance. The system also helps provide a real-time trial financial and recruitment picture with immediate access to data about patient recruitment, site payments and supply inventory.
Several newly developed modules will be demonstrated at DIA, including online site visit trip report design and workflow tools (including electronic signatures), automated event notifications and subscriptions to scheduled reports. An upcoming release planned for later this year will include these features, as well as other new capabilities such as SAE worksheet tracking, additional global reporting options, and enhanced subject visit schedules to handle multiple cohorts or cycles.
DZS/ClinPlus has also partnered with APT, an information technology firm located in Allentown, PA, to host ClinPlus(CTMS) and provide Software-as-a-Service subscription model pricing and accessibility for our global customers. The partnership with APT provides value-added technology services for all of the ClinPlus product line to meet the stringent needs of the pharmaceutical industry for 21CFR Part 11 compliance.
In response to the recent clinical data study standards set out by the Clinical Data Interchange Standards Consortium (CDISC), specifically with regards to the Study Data Tabulation Module (SDTM) and the Analysis Data Model (ADaM), DZS enhanced their SAS-based ClinPlus Report software so that adhering to and properly managing these data standards among workgroups, between departments and across the enterprise could be achieved much more efficiently, resulting in dramatic time and cost savings, increased productivity and earlier visibility to reliable clinical data. ClinPlus Report also touts an extensive template library (50+) for generation of CDISC/ ADaM compliant safety tables and listings for ten data domains with supporting documentation in a validated, standardized way.
According to Bob Borysko, VP of Programming and Development at DZS Software Solutions, "These developments underscore our commitment to helping the life science industry meet the challenges of both regulatory and standards-setting bodies as efficiently and effectively as possible." Added Mr. Borysko "Our goal is to offer robust solutions to help our clients leverage these standards and expedite their clinical trials."
To speak to a product expert or arrange a personalized demonstration, please contact sales&marketing@clinplus.com or follow this link to request specific information or pricing: http://www.clinplus.com/products/clinical-trial-management-software?utm_campaign=CTMS-1.1-Promo&utm_source=Fast%20Pitch%2C%20LinkedIn%20Groups
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. (www.clinplus.com) 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 50 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 every system!
Contact:
Keith W. Ward
Director of Global Marketing
DZS Software Solutions, Inc.
1661 Route 22 West,
Bound Brook, NJ 08805-1258
Office: (732) 764-6969 Ext: 129
Fax: (732) 764-6755
http://www.linkedin.com/profile
kward@clinplus.com
http://www.clinplus.com/
Posted on Tue, Apr 20, 2010
Strategic Alliance between DZS/and APT will facilitate Software-as-a-Service (SaaS) delivery of their recently launched ClinPlus Clinical Trial Management Systems (CTMS) and future Electronic Data Capture (EDC) and Medical Coding applications in a fully validated 21 CFR Part 11 compliant manner.
Bound Brook, NJ - April 19, 2010 - DZS Software Solutions, Inc. and APT Information Technology Consultants of Allentown, PA have formed a strategic alliance for APT to provide clinical information systems management and hosting services via their WebtrialZ offering to enable software delivery as a service (SaaS) for DZS's recently released, web-based clinical trial management software as well as their future EDC and Coding solutions. Both companies plan on demonstrating their solutions at the upcoming ACRP Global Conference in Tampa, FL, April 23rd - 27th. (DZS Booth #529 and APT Booth #229)
SaaS-enabled technologies have gained increased popularity of late because they can be implemented without IT department support, don't require significant up-front capital investment, and eliminate the need for installed servers and the associated maintenance costs. All that's required is an internet connection and browser. Until recently, skeptics have been reluctant to adopt SaaS technology in part because of security concerns. However, using APT's WebtrialZ Services, software applications can be deployed rapidly with the assurance that the data is safe, secure and managed to a level that will meet the 21 CFR Part 11 standards and the most rigorous Pharmaceutical Sponsor audit. APT has extensive experience managing and documenting clinical information systems with services that include the creation and management of IQ/OQ documents for the servers, software and associated equipment, and an established change-management process used to facilitate and document any system changes.
The availability of ClinPlus CTMS in a SaaS delivery model is also an extremely important and timely development for many emerging Life Science organizations struggling with the challenges of improving clinical trial productivity while at the same time reducing expenses. "The appeal of this delivery model is its immediate availability to Life Science companies of all sizes, and its ability to accommodate a wide range of the requirements needed to quickly and effectively deploy the software and get clinical studies up and running in weeks and not months," said Bob Borysko, DZS's VP of Product Development. "By improving global user accessibility and communications, tremendous efficiencies and time-savings can be realized, manual operations can be reduced and redundant data and tasks can be completely eliminated."
To speak to a product expert please contact sales&marketing@clinplus.com or follow this link to request specific information or pricing: http://www.clinplus.com/ctms-landing-clinplus-clinical-trial-management-system-ctms/?utm_campaign=CTMS-ACRP&utm_source=PR-Fastpitch%2C%20Group%20posts
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. (www.clinplus.com) 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 50 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 every system!
Contact:
Keith W. Ward
Director of Global Marketing
DZS Software Solutions, Inc.
1661 Route 22 West,
Bound Brook, NJ 08805-1258
Office: (732) 764-6969 Ext: 129
Fax: (732) 764-6755
http://www.linkedin.com/profile
kward@clinplus.com
http://www.clinplus.com/
About APT
Founded in 1995 in Allentown, PA, APT Information Technology Consultants is a privately held company which focuses on specialized hosting and critical systems management services. APT serves clients throughout North America, Europe, and the world. Our clients include biotech and pharmaceutical companies, as well as a host of new and emerging businesses.
Our staff of experts has substantial technical experience in the pharmaceutical industry. APT's WebtrialZSM Hosting Service allows customers to focus on their day-to-day business and eliminates the hassle of managing an Information Technology infrastructure. APT provides a seamless extension of a client's IT organization controlled by an extensive set of comprehensive SOPs covering every aspect of system implementation and ongoing management.
Our U.S.-based technical support specialists offer a variety of flexible support options. As a recognized industry leader, APT develops and maintains custom infrastructure support plans while using best practice methodology. APT uses state-of-the-art technologies in hardware, software, and connectivity.
Contact:
Jason Gaston, Technical Sales Consultant
Tammy Long Ferry, Business Development Manager
APT Information Technology Consultants
7540 Windsor Drive, Suite 204
Allentown, PA 18195
Office: (610) 366-1100
Fax: (610) 366-7375
webtrialz@aptconsulting.com
http://www.webtrialz.com/
Posted on Wed, Mar 31, 2010
ClinPlus's CTMS system now available in a software-as-a-service (SaaS) delivery model, offering CRO's, Pharma, Biotech and Medical Device organizations cost-effective subscription model pricing, rapid system deployment, scalability, and site set-up flexibility.
Bound Brook, NJ - March 31, 2010 - DZS Software Solutions, Inc. plans on demonstrating enhanced functionality for its recently released (June 2009) CTMS software solution, part of the ClinPlus Solution Suite at the upcoming ACRP Global Conference in Tampa, FL, April 23rd - 27th. (Booth # 529)
In today's competitive drug development environment, two glaring statistics point to a major obstacle in shortening time-to-market and lowering the cost of clinical trials. First, almost half of the cost of bringing a new drug or device to market, or close to $400 million, is accrued during the clinical trial phase. Second, recent studies also indicate that 75 percent of all trials conducted in the United States are behind schedule by one to six months.
Most of these clinical trials involve a large amount of data, both paper-based and electronic, from thousands of patients, hundreds of sites and a multitude of trial administrators - data that must be collected, transmitted, shared, analyzed, and archived. The good news is that with products like ClinPlus CTMS, companies can reap significant cost and time savings with better visibility and efficient management of their clinical trial information.
The availability of ClinPlus CTMS in a SaaS delivery model is also an extremely important and timely development for many emerging Life Science organizations struggling with the challenges of improving clinical trial productivity while at the same time reducing expenses. "The appeal of this delivery model is its immediate availability to Life Science companies of all sizes, and its ability to accommodate a wide range of the requirements needed to quickly and effectively deploy the software and get clinical studies up and running in weeks and not months," said Bob Borysko, DZS's VP of Product Development. "By improving global user accessibility and communications, tremendous efficiencies and time-savings can be realized, manual operations can be reduced and redundant data and tasks can be completely eliminated."
Because of the continuum of disparate functions and business units that typically exist across pharmaceutical companies, CROs and clinical trial sites, SaaS-enabled technologies have gained increased popularity of late because they can be implemented without IT department support, don't require significant up-front capital investment, and eliminate the need for installed servers and the associated maintenance costs. All that's required is an internet connection and browser.
According to Gartner Research, SaaS Delivery within the Enterprise Application Software markets will show consistent growth through 2013, with worldwide SaaS revenue totaling an estimated $14.4 billion based on total software revenue. In 2008 revenue was $6.4 billion.
Until recently, skeptics have been reluctant to adopt SaaS technology in part because of security concerns. However, using virtualization systems, DZS's SaaS model provides Life Science organizations a distinct and self-contained environment to maintain data protection. Data is also preserved through daily incremental backup and weekly full backup. Other benefits include the ability to scale up or down as needed; round-the-clock accessibility, and complete control over study timelines.
To speak to a product expert or a personalized demonstration, please contact sales&marketing@clinplus.com or follow this link to request specific information or pricing: http://www.clinplus.com/ctms-landing-clinplus-clinical-trial-management-system-ctms/?utm_campaign=CTMS-ACRP&utm_source=PR-Fastpitch%2C%20Group%20posts
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. (www.clinplus.com) 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 50 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 every system!
Contact:
Keith W. Ward
Director of Global Marketing
DZS Software Solutions, Inc.
1661 Route 22 West,
Bound Brook, NJ 08805-1258
Office: (732) 764-6969 Ext: 129
Fax: (732) 764-6755
http://www.linkedin.com/profile
kward@clinplus.com
www.clinplus.com
Posted on Tue, Feb 23, 2010
Bound Brook, NJ - February 23, 2010 - The United States Military HIV Research Research Program (MHRP) centered at the Division of Retrovirology, Walter Reed Army Institute of Research (WRAIR), Rockville MD has selected and deployed DZS Software Solutions SAS-based ClinPlus Data Management solution to support their worldwide clinical research program.
MHRP remains at the forefront of the battle against HIV to protect U.S. troops from infection and to reduce the global impact of the disease. While its primary focus is developing a globally effective HIV-1 vaccine, the program provides prevention, care and treatment through the President's Emergency Plan for AIDS Relief (PEPFAR).
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. (www.clinplus.com) 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, 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 every system!
Posted on Wed, Feb 17, 2010
Breakthrough enhancements in ClinPlus Report Engine promise to save SAS programmers significant mahours when producing tables and listings.
Bound Brook, NJ (April 2, 2008) - DZS Software Solutions, Inc. announced their latest release of the ClinPlus Report Engine, Version 7.0
While several enhancements have been made, the most significant by far is the intelligent column-variable stacking and word wrapping. ClinPlus Report users now have the ability to stack variables within columns while retaining logical row integrity even if variable text is wrapped within several columns on multiple levels. Grouping integrity is also maintained during pagination.
Consider the following simple example:
The pressure to produce this type of listing has been building over the last couple of years because so much information can be presented in a concise report that does not span multiple pages. Although, at first glance, this layout appears rather straight-forward, statistical programmers have always found it extremely difficult to near impossible to produce within any reasonable time frame.
However, using ClinPlus Report, simply define your columns, specify the new STACK option and the ClinPlus Report engine will consistently and elegantly produce the layout you expect.
This breakthrough enhancement promises to save our clients hours of programming time for each report produced.
Other enhancements in version 7.0 include:
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Improved Total line placement at the top of groups.
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Improved labeling of SHOW variables
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Improved internal warnings
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Several support issues addressed
Comprehensive system demonstrations are now available by contacting salesandmarketting@clinplus.com.
About ClinPlus Report
ClinPlus Report is SAS® based software designed to create high-quality statistical tables and listings quickly and easily from all types of data. Its unmatched versatility accommodates complex statistical summary tables to simple data listings and is the reason why it has been adopted as a standard by many including several of the top ten pharmaceutical companies.
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. has been providing clinical trials software for data management & analysis to the pharmaceutical industry since 1996. Our ClinPlus suite of products provides the premium quality tools necessary for pharmaceutical companies, contract research organizations (CROs), biotech's, and medical device manufacturers to expedite clinical trials and meet the strict requirements of the FDA. From data collection, coding, analysis, and submission, ClinPlus provides the edge you need to get products to market faster.
Averaging 15 years each in the pharmaceutical industry, DZS software engineers bring several decades of experience in areas such as statistical analysis, clinical data management, and ADE/Drug coding. Our real world experience is incorporated in each system's design and is evident in the many features not found elsewhere.
Posted on Tue, Feb 16, 2010
ClinPlus's latest 3.3 release of their SAS-based data management and coding software promises greater data throughput and greater productivity for the management, analysis and coding of clinical trial data
Bound Brook, NJ (February 15, 2010) - DZS Software Solutions, Inc., developers of the ClinPlus brand of products, and a technology and services leader focused on global clinical trial solutions, announced today they have released ClinPlus® Data Management 3.3, an enhancement to their well established flagship data management, and electronic data capture (EDC) suite.
This SAS-based suite is fully validated under SAS 9.2 and extremely reliable with over seventy new enhancements and fixes. The system also supports 64-bit processing, offering unparalleled performance and speed. The data management software is integrated with ClinPlus Coding software, as well as ClinPlus's Clinical Trial Management (CTMS) and Report Systems; combined, the suite of software delivers greater user productivity and ability to gain early visibility to clinical trial data, manage trial operations, meet trial deadlines and data formatting requirements for New Drug Applications (NDAs) submitted to the FDA and other global regulatory authorities.
Many DZSs clients are currently migrating from 32-bit architecture to the 64-bit architecture to leverage the increased performance. Tami L. Bullen of QST Consultations, Ltd., a Michigan-based independent consulting firm for the medical device and pharmaceutical industries stated that "Using ClinPlus Data Management allows us to keep the data in the same system that we use to analyze it. This eliminates the lengthy procedure of exporting data from the system and converting it to SAS data sets. Using ClinPlus Data Management has definitely increased our productivity by being more efficient in our processes".
ClinPlus Coding is the industry's most powerful coding software and leverages leading-edge Microsoft .NET, SQL technology and the latest changes in dictionary formats and evolving industry guidance. It 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.
ClinPlus Services offers business process consulting and outsourcing for clients wishing to implement, upgrade or migrate to their suite of clinical trial solutions. For more information, please visit the company's website or contact them TOLL-FREE at 1-866-CLINPLUS. ClinPlus offers flexible lease or purchase payment options for those that qualify.
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. (www.clinplus.com) 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, 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 every system!
Contact:
Keith W. Ward, Director of Global Marketing
DZS Software Solutions, Inc.
1661 Route 22 West, Bound Brook, NJ 08805-1258
Office: (732) 764-6969 Ext: 129 Fax: (732) 764-6755
kward@clinplus.com
www.clinplus.com
Posted on Tue, Feb 16, 2010
Romark decides on ClinPlus's Data Management and Medical Coding software for the management of both paper-based and electronically-captured data and medical coding as well as ClinPlus's unparalleled reputation for support.
Bound Brook, NJ - February 8, 2010 - Tampa, Florida-based Romark Laboratories has selected DZS Software Solution's ClinPlus® Data Management and ClinPlus® Coding systems as its software of choice for managing data and medical terminology for upcoming clinical trials.
Romark is currently conducting US and international phase 2 clinical trials of new drugs for treatment of chronic hepatitis C and influenza. The company plans to use the ClinPlus Data Management and Medical Coding software for these trials and for phase 3 trials to be initiated later this year.
Romark ultimately decided on ClinPlus's Data Management and Medical Coding software primarily because key staff members were already trained and familiar with the DZS's industry-proven solutions for the management of both paper-based and electronically-captured data and medical coding as well as the company's unparalleled reputation for support.
"We are working on very aggressive clinical development programs, and we needed a versatile and reliable system that could be implemented quickly," said Marc Ayers, Chief Executive Officer of Romark. "We were very comfortable with our decision to go with DZS, and we were confident they could meet our tight implementation timelines. Additionally, because of our familiarity with SAS and the Data Management and Coding software, we knew study set-up would go rapidly, allowing us to forgo extensive training that would have been required with other systems." ClinPlus Data Management is a SAS-based system that is ideal for CRF tracking, data entry, analysis and review, medical coding and trial reporting. The system can be easily extended to support Electronic Data Capture (EDC) with the use of Citrix.
About Romark Laboratories, LC
Romark Laboratories, L.C. (www.romark.com) is a biopharmaceutical company committed to the discovery and development of innovative new small molecules for treating infectious diseases and cancers.
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. (www.clinplus.com) 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 50 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, 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 every system!
Posted on Mon, Sep 28, 2009
DZS Software Solutions, Inc., developers of the ClinPlus brand of products, and a technology and services leader focused on global clinical trial solutions, today formally announced the launch of its new website found @ www.clinplus.com.
Bound Brook, New Jersey (September 28th, 2009) - The latest release is designed with the overall visitor experience in mind. In addition to the overall experience, the new website heightens ClinPlus brand recognition and promotes its continuously expanding product and services offerings like its recently released Clinical Trial Management System (CTMS). The new Website is a collaboration between DZS's marketing department and "Geeks on Steroids" web design firm located in Columbia, South America.
"Our new website is a great representation of the ClinPlus brand and what it represents. We have made it a point after launching ClinPlus almost 15 years ago to engage our customers at all levels and the intranet has become the one constant in terms of where customers turn for information about a company and its products and services. The web is a powerful tool and in many cases it is the first impression to the customer of what a brand represents both in terms of image and product. We want to immerse new and current customers alike in the ClinPlus experience," says DZS CEO, Doron Steger.
"The Social Network Marketing trend is beginning to make its imprint on nearly every industry and Life Sciences is no exception, as brands look for new avenues to market to their customer base. ClinPlus's new website will serve as a foundation for exploring these emerging new social mediums and support our commitment to creating global brand awareness through thought leadership. It will also serve as gateway for information about industry best practices and DZS products and services," comments Keith Ward, DZS's Director of Global Marketing. What we are announcing today is just the first phase. It will only get more exciting as we continue development and build off the client interest," adds Ward.
Contact:
Keith W. Ward
Director of Global Marketing
DZS Software Solutions, Inc.
1661 Route 22 West,
Bound Brook, NJ 08805-1258
Office: (732) 764-6969 Ext: 129
Fax: (732) 764-6755
kward@clinplus.com
www.clinplus.com
Posted on Tue, Sep 15, 2009
ClinPlus® web-based (CTMS) proves to be best choice for proprietary device technology using trans-cranial laser therapy (TLT) for the treatment of acute ischemic stroke and other neurological diseases and disorders.
Bound Brook, NJ (September 15, 2009) - DZS Software Solutions, Inc., developers of the ClinPlus brand of products, and a technology and services leader focused on global clinical trial solutions, announced today they have entered into an agreement with PhotoThera, Inc, of Carlsbad, CA to provide Clinical Trial Management Software (CTMS) for their upcoming pivotal clinical trial involving transcranial laser therapy (TLT).
PhotoThera selected DZS‘s new web-based CTMS after an extensive RFP process involving over 10 different CTMS solution providers. "After reviewing a variety of competitive CTMS systems, DZS's ClinPlus CTMS emerged as the most logical fit for our needs and budget", said Cindy Croissant, PhotoThera's Director of Clinical Operations. "One of the main reasons we decided on DZS, was the fact that we found the intuitive design of the system to be easy to navigate, which we felt eventually would translate into less training time and less potential for errors and frustration among the system users. We were also impressed with the simple elegance of the system, the attention to detail, and DZS's commitment to configure and deliver a product to meet our unique requirements," added Ms. Croissant.
The ClinPlus CTMS improves site productivity by eliminating redundant systems and existing manual tasks and helps enforce PhotoThera's adherence to trial procedures and regulatory compliance. The system also helps provide a real-time trial financial and recruitment picture with immediate access to data about patient recruitment, site payments and supply inventory. The ClinPlus CTMS will enable PhotoThera Clinical Research and Engineering professionals to be proactive rather than reactive, and control and manage trials in ways not possible when only spreadsheets or manual processes are used. The system also alerts users of out-of-window patient visits, late monitoring visit reports, documents due to expire, and other unresolved monitoring issues. And because the system is web-based, all that's needed is an internet connection and a computer. This allows users around the world to access data immediately and make changes as needed, preventing frustration and errors which commonly happen when one user makes and distributes all changes. As a hosted solution ClinPlus CTMS offers low start-up costs of between $50.-120./month per user, with very few IT implementation issues, robust data security, and unmatched levels of efficiency. And, by improving overall efficiency, ClinPlus CTMS helps reduce overall product timelines and the ability to meet trial deadlines.
Posted on Mon, Jun 15, 2009
ClinPlus® expands their existing suite of clinical trial software and service solutions to include web-based Clinical Trial Management System (CTMS)
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Bound Brook, NJ (June 15, 2009) - DZS Software Solutions, Inc., developers of the ClinPlus brand of products, is a technology and services leader focused on global clinical trial solutions. DZS today announced they will be unveiling new branding as well as a new Clinical Trials Management System (CTMS) and a number of exciting new features and functionality to their existing ClinPlus Solutions Suite of products that include ClinPlus® Data Management and ClinPLus ®Coding.
Until recently, many research organizations have delayed the adoption of new CTMS technology due to the complexities of implementing such a system across their enterprise. Technological change of this scale that affects all areas of an organization requires new workflows and changes in inefficient, but well established manual routines can be extremely difficult and time-consuming to accomplish.
DZS‘s new web-based ClinPlus CTMS, based on Microsoft .NET technology makes the utilization and integration of information across the enterprise much easier than in the past. The ClinPlus CTMS dramatically improves site productivity by eliminating redundant systems and manual tasks and helps enforce adherence to trial procedures. The system also provides a real-time trial financial and recruitment picture with immediate access to data about patient recruitment and reimbursement. ClinPlus CTMS is designed to track the status of people, events, data and finances and documentation involved in and required for a clinical trial. It tracks planned activities and events to ensure that they occur, and notifies users about upcoming activities and events. The system allows research professionals to be proactive rather than reactive where possible, and enables the control and management of clinical trials in ways not possible when only spreadsheets or manual processes are used. The ClinPlus CTMS can proactively warn organizations of out-of-variance patient visits, deficient regulatory documents or documents due to expire, and unresolved monitoring issues. This capability enables resolution of queries within minutes rather than hours needed to find and possibly miss these issues. And because the system is web-based, all that's needed is an internet connection and a computer. As a hosted solution it offers low start-up costs, very few IT implementation issues, robust data security and unmatched levels of efficiency. And, by improving overall efficiency, ClinPlus CTMS helps reduce product timelines and meet trial deadlines.
DZS/ClinPlus will be exhibiting their suite of products at the San Diego Convention Center, Booths 1024-1026 from 9AM Monday June 22nd through 4:00PM Wednesday June 24th. Prospects are encouraged to arrange comprehensive system demonstrations by contacting: salesandmarketting@clinplus.com.
About 45th Annual DIA Meeting.
The DIA Annual Meeting is the biopharmaceutical industry's largest global, multidisciplinary event. The 45th DIA Annual Meeting's focus is 'Better Medicines: Improving Safety with Every Step' and is being held June 21-25, 2009 at the San Diego Convention Center in San Diego, California. For the first time ever, DIA is offering LIVE online content from the Annual Meeting. For more information on the meeting, visit http://www.diahome.org.
About DZS Software Solutions, Inc.
DZS Software Solutions, Inc. (www.clinplus.com) 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 50 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, 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 every system!
Contact:
Keith W. Ward
Director of Global Marketing
DZS Software Solutions, Inc.
1661 Route 22 West,
Bound Brook, NJ 08805-1258
Office: (732) 764-6969 Ext: 129
Fax: (732) 764-6755
kward@clinplus.com
www.clinplus.com