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chemical information access Applications

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    EH&S Regulatory Compliance Management for Electronics And Medical Devices

    Few industries face the mounting challenges and scrutiny of expanding environmental compliance requirements, ecological mandates, consumer expectations and NGO watch groups as much as electronics and medical device manufacturers. Even before the Sony PlayStation cadmium crisis, the entire supply chain has been inundated by an ever-expanding myriad of legislation, ranging from the EU Directives on waste electrical and electronic equipment (WEEE), the restriction of hazardous substances (RoHS) and the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) to US legislation on conflict minerals. The depth and amount of information that suppliers must access, evaluate, compile, integrate and disclose is growing exponentially.

    By 3E Company based in Carlsbad, CALIFORNIA (USA).

  • SDS Authoring and Generation

    The SDS Authoring and Generation module manages the creation, distribution, and storage of Safety Data Sheets (SDSs). Designed to meet increasingly stringent regulatory requirements of a number of jurisdictions both domestic and foreign, the module dramatically reduces the cost and liability associated with typical SDS management programs. . By 2015, all SDS documents and labels must comply with the Globally Harmonized System (GHS) classification standards. Features include: • Automatic flagging and documentation of first shipments, revised SDS, and no SDS within one year • Masked complexity (with access to full detail) • Protection of trade secrets by user-defined percent ranges, and the ability to hide proprietary chemical information • Cross referencing of business operating languages • Ability to update multiple SDS simultaneously SDS Authoring and Generation can be purchased as a standalone solution or as part of the Q EHS compliance software package.

    By Quantum Compliance based in Ann Arbor, MICHIGAN (USA).

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