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Keynote Address by Jigar Shah, CEO of Carbon War Room and Founder of SunEdison

Charlotte, NC — April 27, 2010 — Camstar Systems, Inc. announced today that The Summit on Solar Quality will be held in Santa Clara, CA, on June 29, 2010. Thought leaders across the Solar Industry will be represented at this educational event. Topics will focus on the state of quality in the solar industry, and approaches to accelerate grid parity.

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Leading Broadband Wireless Manufacturer Highlights Flexibility and Proven Quick Deployment as Key Advantages over Competing Solutions

CHARLOTTE, N.C. (April 22, 2010) – Camstar Systems, Inc. announced today that REMEC Broadband Wireless, a manufacturer and EMS provider of broadband wireless devices, components, and sub-systems including transceivers and microwave radio ODUs, has selected Camstar’s ElectronicsSuite™, configured for the Electronics industry on the Camstar Enterprise Platform, to support its manufacturing, quality and customer satisfaction goals.

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Process improvement is routinely portrayed as a journey, so any tool that tips the scales in favor of the journey taker is well worth bringing along.

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May 6, 2010
1:00pm EDT

eDHR is not just taking your paper DHR and converting it into an electronic format…its modeling your process in a structured way so that there are automated preventive controls which enforce proper procedure so that you manufacture and test/inspect your product right, the first time, every time. And compliance becomes a by-product of this approach.

In this session you will see a live demonstration of Camstar’s MedicalDeviceSuite^TM, with a focus of eDHR/EBR; you will hear how proactive companies are using eDHR to reverse the negative adverse event trend; and you will learn how an eDHR system can enable you to:

• Prevent avoidable issues through automated enforcement of the 5 Ms (Man, Material, Method, Machine, Measurement)
• Reduce Adverse Quality Events (Recalls, MDRs, CAPAs, Complaints, etc)
• Automatically collect quality and manufacturing data throughout the supply chain
• Improve Operational Efficiencies and Cycle Times and inventory by streamlining operations (by removing not value added inspections/verifications, etc) and detailed visibility to WIP status
• Reduce New Product Introduction timelines and Risk by feeding existing product information into development to optimize design, process, and controls.
• Reduce Cost of Compliance and Cost of Poor Quality.
• Capture entire ‘as-built’ and ‘as-maintained’ Device History Record including full product genealogy/traceability
• Maintain complete audit trails to meet FDA requirements
• Reduce internal/external audit risk

Learn More and Register

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