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  2. Registration, Evaluation, Authorisation and Restriction of ...

    en.wikipedia.org/wiki/Registration,_Evaluation...

    Such submission is a mandatory part of the registration process. Under certain circumstances the performance of a chemical safety assessment (CSA) is mandatory and a chemical safety report (CSR) assuring the safe use of the substance has to be submitted with the dossier. Dossier submission is done using the web-based software REACH-IT.

  3. REACH authorisation procedure - Wikipedia

    en.wikipedia.org/wiki/REACh_authorisation_procedure

    The formulation of a mixture is considered as a use under REACh and the substance of the Annex XIV is only subject to authorisation if it exceeds the required concentrations. If the production of an article may require an authorisation at some point, finished articles themselves do not require an authorisation to be put on the market, even ...

  4. Council for International Organizations of Medical Sciences

    en.wikipedia.org/wiki/Council_for_International...

    This publication laid the groundwork for CIOMS' 1982, 1993, 2002, 2009, and 2016 versions of International Ethical Guidelines for Health-Related Research Involving Humans. [3] These guidelines have been praised for including diverse stakeholders from low- and middle-income countries, compared to the Declaration of Helsinki written by physicians ...

  5. Not 1. Not 2. Not 3. Not 4. 5 winter storms could deliver ...

    www.aol.com/not-1-not-2-not-164201387.html

    The second of five storms that will slam the eastern half of the United States with snow and ice over a two week period is on the way – and this one has more snow than the first.

  6. New Drug Application - Wikipedia

    en.wikipedia.org/wiki/New_Drug_Application

    A new drug application in the 1930s for sulfapyridine to the United States Food and Drug Administration. The Food and Drug Administration's (FDA) New Drug Application (NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new pharmaceutical for sale and marketing.

  7. Production part approval process - Wikipedia

    en.wikipedia.org/wiki/Production_part_approval...

    PPAP is a series of documents gathered in one specific location (a binder or electronically) called the "PPAP Package". The PPAP package is a series of documents which need a formal certification / sign-off by the supplier and approval / sign-off by the customer. The form that summarizes this package is called PSW (Part Submission Warrant).

  8. Global Reporting Initiative - Wikipedia

    en.wikipedia.org/wiki/Global_Reporting_Initiative

    The reporting techniques were encouraged to rely on recognized frameworks such as GRI's Sustainability Reporting Guidelines, the United Nations Global Compact (UNGC), the UN Guiding Principles on Business and Human Rights, OECD Guidelines, International Organization for Standardization (ISO) 26000 and the International Labour Organization (ILO ...

  9. Wikipedia : Did you know/Guidelines

    en.wikipedia.org/.../Guidelines

    This is a complete handbook of all of DYK's guidelines and standard practices. It is more helpful as a reference than a guide – if you're looking for a guide on how to do a specific job, see the reviewing, prep building, and admin instructions. To some extent, DYK approval of a nomination is a subjective process.