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The product data submittal usually consists of the manufacturer's product information. The information included in this submittal are: Manufacturer, trade name, model or type number and quantities: This information is necessary to compare the submitted item with the specified products and acceptable products listed, in the specification and addenda.
Regulated Product Submission (RPS) is a Health Level Seven (HL7) standard designed to facilitate the processing and review of regulated product information. [1] RPS is being developed in response to performance goals that the U.S. Food and Drug Administration (FDA) is to achieve by 2012, as outlined in the Prescription Drug User Fee Act (PDUFA). [2]
Product data management is the use of software or other tools to track and control data related to a particular product. The data tracked usually involves the technical specifications of the product, specifications for manufacture and development, and the types of materials that will be required to produce goods. The use of product data ...
Level 1 – Part Submission Warrant (PSW) only submitted to the customer. Level 2 – PSW with product samples and limited supporting data. Level 3 – PSW with product samples and complete supporting data. Level 4 – PSW and other requirements as defined by the customer.
Document management systems are deployed for archiving, and product data management involves the management of structured, technical data for such applications as parts diagrams and lists. Content management systems are more commercially oriented and provide a framework for knowledge management or informational service offerings through the ...
Manage paperwork: Scan barcodes of appliances and purchases in the home, which allows you access to manuals and warranty information; photograph product receipts along with photos and video
How We Use Data to Provide More Effective Advertising As noted above, we use the data we collect or receive about users' online activities to help us show ads for products or services users are likely to be interested in and make the advertising we provide more effective. Some of the ways we do this are:
In medtech, building upon the 15 major product launches in 2024, we anticipate a submission to the FDA for Impella ECP regulatory approval, continued progress on our Ottava robotic surgical system ...