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  • Medical Device Link .
    An outsource packaging services company has invested in the medical technology side of its business to the extent that it has created a dedicated new business entity for this sector. IL-MedTec AG (Burgdorf, Switzerland; ), a unit of Ivers-Lee AG, offers packaging and supplementary services
  • Experiences With the Fabrication and Service Behavior of Components Made of TI and ZR in the Chemical Process Industry (.pdf)
    with a significant surface area, especially if localized corrosion phenomena may. occur. Welded coupons should always been used if there will ever be welds in the plant. In some. cases, even supplementary electrochemical or other highly sophisticated testing may be advisable to. reach an optimum result
  • The New CK Series Rotating Union Has Done an Excellent Job!
    external cooling system. The new CK series has been installed in numerous calenders across Europe, Asia and America, and it has proven to be a successful solution for every installed application. When considering the TCO and not the product "rotating union" itself, the supplementary services rendered
  • Creating Equipment that Meets Carrier Requirements using Open Standards (.pdf)
    ), International Exchange Carriers (IXC), and other networks operators prior to deployment in their networks. In addition to meeting NEBS requirements, some of the North American carriers require additional testing to be performed, most commonly known as "NEBS Supplementary Requirements". European
  • Medical Device Link .
    ), with Amendments 1 (1991-11) and 2 (1995-03). Technology-related safety requirements addressing medical systems, electromagnetic compatibility (EMC), x-ray radiation, and programmable systems are covered by supplementary standards. A further group of standards covers device-specific safety
  • Medical Device Link .
    such an investigation may be required are indicated in ISO 10993-1, Table 2: Guidance for Supplementary Evaluation Tests. Specifically, such testing should be considered for a device that will have permanent contact (longer than 30 days) with tissues, either as an implant or as an externally
  • Medical Device Link .
    device once it was sent outside the manufacturer�s premises and control, and before it was sold to the end-user. This supplementary period was a late concession intended to assist distributors with surplus stocks of high-cost equipment that they would have been unable to sell before
  • QQ-S-365 Silver Plating: Electrodeposited - General Requirements
    be of the following types, as specified (see 3.3.4 and 6.3): Type I – Matte Type II – Semi-bright Type III – Bright 1.2.2 Grades. Silver plating shall be of the following grades, as specified (see 3.4.5 and 6.1.3): Grade A – With supplementary tarnish-resistant treatment (chromate treated) Grade B – Without
  • Medical Device Link .
    of the individual risks. The clause reads as follows: Currently, the supplementary document ISO/IEC 14971 Amendment 1 is in its final stages of development; no further technical changes will be made. This supplement does not change the normative requirements, but does provide rationales for them. With regard
  • Medical Device Link . Sterilization Firms Strive to Cut Costs, Turnaround Times
    control system suitable for use with all types of gamma irradiation plants. A flexible, modular design allows nearly any combination of in-cell control, automated dosimetry, and product tracking with the use of additional supplementary modules. "This enables us to tailor a control system to satisfy