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To drive costs out of the health-care sector, medical logistics providers are adopting supply chain management theories. This organizational chart is as follows and separated into three key areas. Medical Materiel [2] Facilities Management. Biomedical Engineering or Clinical Engineering; These areas are managed by a qualified Director of Logistics.
The distribution of medications has special drug safety and security considerations. [1] Some drugs require cold chain management in their distribution. [2]The industry uses track and trace technology, though the timings for implementation and the information required vary across different countries, with varying laws and standards.
[14]: 2 Supply chain management was then further defined as the integration of supply chain activities through improved supply chain relationships to achieve a competitive advantage. [12] In the late 1990s, "supply chain management" (SCM) rose to prominence, and operations managers began to use it in their titles with increasing regularity.
ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.
Medical devices first came under comprehensive regulation with the passage of the Federal Food, Drug, and Cosmetic Act of 1938 (FD&C), [9] which replaced the earlier Pure Food and Drug Act of 1906. The FD&C allowed the FDA to perform factory inspections and prohibited misbranded marketing of cosmetic and therapeutic medical devices. [10]
Medical facility rooms can collect data from transmissions of RFID badges worn by patients and employees, as well as from tags assigned to items such as mobile medical devices. [89] The U.S. Department of Veterans Affairs (VA) recently announced plans to deploy RFID in hospitals across America to improve care and reduce costs.
The practice of reusing medical devices labeled for only one use began in hospitals in the late 1970s. [8] After a thorough review by the U.S. FDA in 1999 and 2000, [8] the agency released a guidance document for reprocessed SUDs that began regulating the sale of these reprocessed devices on the market, [9] under the condition that third-party reprocessors would be treated as the manufacturer ...
BMK serves companies from different industries such as medical devices, automotive, metering, consumers, rail technology or telecommunications. Apart from manufacturing and development BMK also focuses on product life cycle management, supply chain management, material management and after sales services.
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