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The High Costs of Non-compliance for Manufacturers
What manufacturers must realize is that through efforts to comply with regulatory standards, they can make their manufacturing operations more competitive

medical waste disposal regulations  implanted medical equipment Infected medical equipment at end-of-life Where Compliance Strategies Are Working The following sections provide insights into where compliance strategies are working, highlighting how manufacturers sometimes turn extensive process reengineering and high costs into a lasting competitive advantage and often, cost and efficiency advantages. Reorienting Supplier Relationships Toward Compliance Intel's many efforts at RoHS compliance has permeated their supply chains, enabling Read More...
Electronic Medical Records (EMR) for the Health Care Industry
Electronic Medical Records (EMR) assists physicians and other clinicians document patient care for current visits and provides access to patient clinical history. Sometimes may be referred to as co...
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Documents related to » medical waste disposal regulations


Mercury Medical: A Health Care Manufacturer Improves Reporting and Analysis with IBM Cognos Express
Read how Mercury’s users can now create the most critical reports that they were previously relying on a legacy reporting platform to produce. These include

medical waste disposal regulations  Medical: A Health Care Manufacturer Improves Reporting and Analysis with IBM Cognos Express Read how Mercury’s users can now create the most critical reports that they were previously relying on a legacy reporting platform to produce. These include sales commissions, weekly sales, a rolling 12-month sales report, and an inventory summary report. Read More...
Going Lean Step By Step with IFS Applications
In the relentless pursuit of profitability and competitiveness, more and more companies are turning to lean manufacturing to reduce or eliminate waste in their

medical waste disposal regulations  Lean Step By Step with IFS Applications In the relentless pursuit of profitability and competitiveness, more and more companies are turning to lean manufacturing to reduce or eliminate waste in their production processes. Once confined to the automotive industry, lean principles are becoming standard operating procedure in many industries today. The reason is simple: When implemented with a good performance management system, lean principles have a proven track record of operational and strategic Read More...
Datalliance Sees Strong Growth in First Half of 2013
Datalliance, provider of a software-as-a-service (SaaS) vendor managed inventory (VMI) platform for the consumer goods, industrial, medical device, and other

medical waste disposal regulations  the consumer goods, industrial, medical device, and other markets, reports continued strong growth. Datalliance reports that through the first 6 months of 2013, it saw a 25% increase in year-over-year revenue from 2012. Continuing this pace through the rest of the year would result in Datalliance reportedly seeing its ninth straight year of 20%+ growth. This comes as Datalliance is expanding in Europe, and comes on the heels of updates to its VMI solution in January and May of this year. Datalliance CEO Read More...
Extending SAN Connectivity for Engenio Arrays
The storage industry provides an abundance of white papers discussing the ever-changing data management and retention regulations, the need for business

medical waste disposal regulations   Read More...
Encryption Made Easy: The Advantages of Identity-based Encryption
The growing list of regulations for protecting data in virtually every size organization and industry means enterprises are being pressed hard to find effective

medical waste disposal regulations   Read More...
Inventory (Out of) Control
In a market as competitive as the chemicals industry, providing high quality products to clients quickly and efficiently while meeting the rigorous regulations

medical waste disposal regulations  Deacom ERP,chemicals industry,tracking inventory,inventory,sales forecasting,enterprise resource planning,ERP Read More...
Medical Device Manufacturer Manages Efficient Operation with Sage ERP X3
UreSil, a manufacturer of specialized health care products, feared its legacy manufacturing resource planning (MRP) software was hindering efficiency and

medical waste disposal regulations  Device Manufacturer Manages Efficient Operation with Sage ERP X3 UreSil, a manufacturer of specialized health care products, feared its legacy manufacturing resource planning (MRP) software was hindering efficiency and compliance. The Sage ERP X3 enterprise resource planning (ERP) came to the rescue, and after a formal ERP training program, full implementation required only one week. All processes, including tracking and inventory, are now streamlined, flexible—and compliant. Read More...
Delivering Information Transparency with Service Parts Optimization
Jabil Global Services, a subsidiary of Jabil Circuit provides repair and warranty solutions to companies in computers, communications, medical equipment. To

medical waste disposal regulations  companies in computers, communications, medical equipment. To meet the demand for next day and same day returns, it needed to replace its in-house operations management system with a scalable and robust system. Learn how it used Click Commerce’s reverse logistics and depot repair solutions to manage its advanced exchanges and warehouse fulfillment, and credit receiving processes. Read More...
RFID in Healthcare--A Whole Industry of Value
This article talks about recent and expected FDA regulations and how RFID can help meet those requirements while improving supply chain performance.

medical waste disposal regulations  such as food, pharmaceuticals, medical devices, etc., in pursuit of industry best practices. $49 billion of imports of pharmaceuticals enter this country every year. The pressure is on from consumers and industry to protect their own interests. These represent sometimes conflicting goals of protection. Protect the consumer, yet protect brand integrity and the more political objectives (protect my profit margins). FDA and its stakeholders and lobbyists, and the ecosystems of industries around it have been Read More...
Introduction to Regulatory Compliance for Learning Management Systems
Companies dealing with industry or government regulations are often required to meet specific standards for system security, audit trails, and verification of

medical waste disposal regulations   Read More...
Electrical Efficiency Measurement for Data Centers
Data center electrical efficiency is rarely planned or managed. The unfortunate result is that most data centers waste substantial amounts of electricity. Today

medical waste disposal regulations  Efficiency Measurement for Data Centers Data center electrical efficiency is rarely planned or managed. The unfortunate result is that most data centers waste substantial amounts of electricity. Today, it is both possible and prudent to plan and measure data center efficiency. In addition to reducing electrical consumption, efficiency improvements can bring higher IT power densities. Learn how to describe, measure, and evaluate data center efficiency. Read More...
Complying with US FDA Title 21 CFR Part 11 for the Life Sciences Industry
Compliance with US FDA regulations is a market requirement. Thus, among the nearly 1,500 installations of mySAP ERP software among pharmaceutical, medical

medical waste disposal regulations  ERP software among pharmaceutical, medical diagnostics and devices, and biotechnology companies worldwide, it is vital to be aware of the functions and features of mySAP ERP that demonstrate technical compliance with US FDA 21 CFR Part 11 Electronic Records; Electronic Signatures; Final Rule. Read More...
PTC Submits Test Data to FDA’s Global UDI Database
Working with the FDA and major medical device manufacturers, PTC has developed a Global Unique Device Identifier Database (GUDID) submission solution that such

medical waste disposal regulations  from the misidentification of medical devices.   Medical device manufacturers need to implement compliant processes and technology to meet the UDI requirements and avoid any potential negative consequences. The FDA’s first UDI compliance deadline for high-risk Class III devices is September 24, 2014. High-risk devices are identified as the most complex, life-sustaining, in-body electronic medical devices—these include pacemakers, defibrillators, vascular stents, and ventilators.   This compliance ca Read More...
Implementing Medical Manufacturing Technology to Improve Operations and Control Costs
US manufacturers spend over $25 billion every year on product warranty claims. For medical equipment manufacturers, complex government regulations play a large

medical waste disposal regulations  Medical Manufacturing Technology to Improve Operations and Control Costs US manufacturers spend over $25 billion every year on product warranty claims. For medical equipment manufacturers, complex government regulations play a large part in the rising costs of warranty. Learn how manufacturing technology can help improve product quality and minimize the burden of warranty costs by creating records that can be tapped by lawyers, or by the companies themselves, when faced with warranty issues. Read More...

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