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As the result of a number of recent incidents caused by inappropriate handling of reactive chemicals, CCPS initiated a project in 2001 to develop additional management guidelines for reactive hazards. A CCPS technical steering committee documented the urgent need for... [Pg.395]

A description of committee documents, including what items go out with a meeting agenda and what items should be describe in meeting minutes... [Pg.81]

WS8] BPMI. 2002. BPML 1.0 specification, http //www.bpmi.org/bpml-spec.htm [WS9] OASIS. 2005. Web Services Business Process Execution Language Version 2.0. http / / www. oasis-open, org / committees/documents. php wg abbrev=wsbpel... [Pg.450]

Design Engineer. Whether an employee or a contractor, the design engineer shall provide to the project manager and to the review committee documentation including... [Pg.322]

Notification to ethical committee Documentation of scientific knowledge on the active ingredient Strictly small scale Manufacturing according to c-GMP/PIC guidelines Responsibility, obligation and duty of care attributed to physician and pharmacist Liability Notification... [Pg.38]

On the problems concerning the production of soda, see for instance Municipal Archive Utrecht, Archives Health Committee, documents dated 7 September 1863 and 27 December 1865. [Pg.179]

To efficiendy drive the development of improved substrate materials, the limiting values of birefringence have to be known this is especially tme for WORM and EOD(MOR) substrate disks. These limit values were laid down by the ANSI (American National Standard Institute) Technical Standard Committee (186—188). For 5.25 in. WORM disks, the ANSI document X 3 B 11/88-144 recommends a maximum LEP value of 9% this corresponds to an optical path difference perpendicular to the plane of the disk of not more than 80 nm/mm (double path). For 5.25 in. EOD(MOR) disks, more stringent conditions apply (ANSI-document X 3 B 11/88-049), which also allow calculation of the allowed range. [Pg.156]

Another useful approach is to attempt to get a broad review of the specification draft by operations, maintenance, and engineering. The specification must have an author who can write the basic document and who later edits the draft into the scope and language of the final specification. Single authorship, with committee review, is preferred over committee authorship. Only in rare instances is vendor participation in the specification authorship really justified, except in partnership relationships. [Pg.443]

Letters of intent can be the cause of problems, and there are varying views as to their validity. These are sent in advance of contractual documents, being signed because either the documents are not fully prepared or a decision has not yet been confirmed. For example, in local government a bid may have been accepted by a committee but needs ratification by the full council, which can be up to six weeks later. It is rare for a council to overturn a decision made by a committee, but it does happen. In an attempt to expedite matters, it is common policy to... [Pg.91]

Temperatures on ITS-90, as on earlier scales, are defined in terms of fixed points, interpolating instruments, and equations that relate the measured property of the instrument to temperature. The report on ITS-90 of the Consultative Committee on Thermometry is published in Metrologia and in the Journal of Research of the National Institute of Standards and Technology The description that follows is extracted from those publications.3 Two additional documents by CCT further describe ITS-90 Supplementary Information for the ITS-90, and Techniques for Approximating the ITS-90.4... [Pg.618]

Not all problems were solved, however, and different usages were encountered on the two sides of the Atlantic. A joint British-American committee was therefore set up, and in 1952 it published Rules for Carbohydrate Nomenclature [18]. This work was continued, and a revised version was endorsed in 1963 by the American Chemical Society and by the Chemical Society in Britain and published [19]. The publication of this report led the IUPAC Commission on Nomenclature of Organic Chemistry to consider the preparation of a set of IUPAC Rules for Carbohydrate Nomenclature. This was done jointly with the IUPAC-IUB Commission on Biochemical Nomenclature, and resulted in the Tentative Rules for Carbohydrate Nomenclature, Part I, 1969 , published in 1971/72 in several journals [1]. It is a revision of this 1971 document that is presented here. In the present document, recommendations are designated 2-Carb-n, to distinguish them from the Carb-n recommendations in the previous publication. [Pg.49]

A five-step process is used to develop new guidance documents (see Figure 2.12). The process is initiated by presenting a concept paper to the Steering Committee. [Pg.38]

During the course of its conduct, the sponsor may need to amend a clinical trial, as a consequence of the emergence of new information. If the amendments are deemed to be substantial, in that they may impact on the safety of trial subjects, or change the interpretation of the scientific documents in support of the conduct of the trial, or are otherwise significant, the sponsor shall notify the Competent Authority and the Ethics Committee, using a Trial Amendment Form. The Ethics Committee are permitted 35 days to approve the amendment. [Pg.87]

Dated, documented approvai / favourabie opinion of Institutional Review Board / Independent Ethics Committee... [Pg.90]

In several studies of toxicity, no adverse effects were documented in monkeys or humans. Taking into account data showing that lutein was not genotoxic, had no structural alert, did not exhibit tumor-promoting activity, and is a natural component of the body (the eye), the Scientific Steering Committee concluded there was no need for a study of carcinogenicity. [Pg.573]

For the validation of chromatographic methods a good starting point can be found in the EURACHEM/ WELAC document on Accreditation of Chemical Laboratories [30]. ASTM Committee E19 on Chromatography covers all forms of chromatography including gas, liquid, ion and supercritical chromatography. [Pg.176]

Finally, some further documents have been developed by the separate inspectors groups (which report via the European Union s Pharmaceutical Committee), and these can be found in the What s New or the Archive section of the Enterprise DG web site. [Pg.645]


See other pages where Committee documents is mentioned: [Pg.358]    [Pg.110]    [Pg.188]    [Pg.358]    [Pg.110]    [Pg.188]    [Pg.21]    [Pg.510]    [Pg.150]    [Pg.156]    [Pg.197]    [Pg.6]    [Pg.82]    [Pg.9]    [Pg.155]    [Pg.601]    [Pg.249]    [Pg.60]    [Pg.632]    [Pg.645]    [Pg.780]    [Pg.781]    [Pg.781]    [Pg.783]    [Pg.801]    [Pg.173]   
See also in sourсe #XX -- [ Pg.184 , Pg.185 , Pg.186 , Pg.187 , Pg.188 , Pg.189 ]




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