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Camstar Announces Its Medical Device Suite(TM) v4.1; Manufacturing Execution and Quality System Provides Control and Performance Management Needed to Eliminate Scrap, Shorten Lead Times and Reduce Risk.


CHARLOTTE, N.C. -- Camstar, the established leader in providing Enterprise Manufacturing Execution and Quality Systems for Life Sciences and other global manufacturers, today announced the release of its new Medical Device Suite(TM) v4.1. Powered by the company's InSite MES (Manufacturing Execution Software) Software that provides real time access to plant activities that include equipment, labor, orders and inventory. An MES integrates the data with enterprise resource planning (ERP) systems so that management has complete control of  framework, Medical Device Suite further accelerates the implementation process for medical device and diagnostics manufacturers. It is the most widely used manufacturing system in the medical device and diagnostics industry, and Camstar's customers include most of the top medical device manufacturers - a number of whom are taking advantage of the Medical Device Suite v4.x family.

Medical Device Suite v4.1 offers the best of both worlds: Industry-specific out-of-the-box functionality plus business rules configurations (not coding). The solution features complete and easily retrievable manufacturing audit trail and electronic device history records, electronically managed specifications and procedures that eliminate human error in manufacturing, automatic detection and control of non-conforming material and test results, structured data for failure and root cause analysis, and a rapid implementation methodology.

Camstar has worked directly with its Life Sciences customers to determine what features will bring them the most benefit. According to according to
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Specifically, Camstar's Medical Device Suite v4.1 includes enhancements to its flexible work-in-process tracking; lot and order dispatching; 21 CFR CFR

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 Part 11 electronic signatures; electronic procedures; operator training and certification; equipment maintenance; non-conformance management; label printing; retrieval of externally managed specification documents; and a number of frequently-requested standard reports. Standard, configurable user interfaces are 100% thin client, so no downloads are required on workstations. An updated Standard Validation Package accompanies all releases of Camstar's applications for regulated industries.

"At Camstar, we focus on customers deriving the most value in the shortest time," said Scott Jones Scott Jones may refer to:
  • Scott Jones (soccer)
  • Scott Jones (rugby league footballer)
  • Scott A. Jones
, Vice President of Development at Camstar. "InSite and Medical Device Suite go beyond a services oriented architecture (SOA (1) (Start Of Authority) The first record in a DNS zone file. See DNS records.

(2) (Service Oriented Architecture) The modularization of business functions for greater flexibility and reusability.
) and offer a true Manufacturing Services Architecture. It takes advantage of the best leading edge technologies such as web services (1) Loosely, any online service delivered over the Web. Such usage appears in articles from non-technical sources, but not in IT-oriented publications, because definition #2 below describes the correct use of the term. , a flexible data model and configurable user interfaces, all of which dramatically reduce deployment and validation time."

Accompanying Medical Device Suite v4.1 is Rapid eDHR(TM) v4.1. Rapid eDHR comprises a subset of Medical Device Suite features which quickly impart electronic control and visibility to device history records.

Camstar customers who wish to learn more about Medical Device Suite v4.1 should contact Customer Support at insitesupport@camstar.com.

About Camstar Systems, Inc.

Camstar is a leading provider of enterprise manufacturing execution and quality systems. Camstar's InSite and Medical Device Suite applications manage, monitor, and synchronize manufacturing activities across globally distributed plants, and integrates them in real-time with core business processes. Rapid to implement, they provide the manufacturing control needed to help eliminate scrap, rework re·work  
tr.v. re·worked, re·work·ing, re·works
1. To work over again; revise.

2. To subject to a repeated or new process.

n.
, paperwork errors and redundant checks. As a result, manufacturers improve yields and product quality, shorten lead times and reach volumes quickly, respond to changing demand, and reduce the cost of compliance. More than 100 leading companies, including Johnson & Johnson, Roche, Tyco, CIBA Vision To meet Wikipedia's and conform with our NPOV policy, this article or section may require cleanup.
The current version of this article reads like an advertisement.
Please discuss this issue on the . is available.
, ZOLL, Zeiss, BIOTRONIK, Kinetic Concepts, IBM (International Business Machines Corporation, Armonk, NY, www.ibm.com) The world's largest computer company. IBM's product lines include the S/390 mainframes (zSeries), AS/400 midrange business systems (iSeries), RS/6000 workstations and servers (pSeries), Intel-based servers (xSeries) , Kodak, AMD (Advanced Micro Devices, Inc., Sunnyvale, CA, www.amd.com) A major manufacturer of semiconductor devices including x86-compatible CPUs, embedded processors, flash memories, programmable logic devices and networking chips. , Philips and Hitachi rely on Camstar as a trusted software partner.
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Publication:Business Wire
Date:May 1, 2006
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