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Consent limits

Listing gaseous emissions, concentrations, smoke characteristics prevailing winds and exposed zones toxicity or nuisance potential effects of synergism or poor atmospheric dispersing conditions. Consent limits. [Pg.353]

Listing effluents, their analyses and discharge from processes. Querying flammability, corrosivity, toxicity, miscibility, reactivity. Checking the reliability of treatment and analysis. Consent limits. [Pg.353]

A major issue for manufacturing processes is the need to minimise the generation of waste, whether it be solid, liquid or gaseous. The reasons for this are two-fold Firstly the need to operate within agreed regulatory consent limits for emissions and waste disposal, and secondly the increasing cost of waste generation and treatment. [Pg.17]

The imposition of consents, limits and authorisations had until recently limited impact on the overall running of a chemical business. As the true effects and implications associated with environmental legislation have developed, the industry has realised that change is necessary. The industry has started to move away from its closed door policy, and become pro-... [Pg.74]

It is of interest to note that during 1976 the arithmetic mean lead content of lead works emissions examined by HM Alkali Inspectorate was 0.011 g mT. It was also noted in the report of the Inspectorate [7] that at the Avonmouth primary lead-zinc-cadmium smelter of Commonwealth Smelting Ltd. (with a capacity of 40 000 tonne of lead annually), emission of lead was about 4 kg h in 1976, compared with a consent limit of 5.4 kg h . ... [Pg.94]

To meet the consent limits and reduce the polluting load and hazardous substances to acceptable levels, most industrial facilities carry out some form of wastewater management and treatment. The simplest form of treatment entails settlement for removal of suspended solids. In such a case, addition of a high molecular weight polyelectrolyte based on polyacrylamide as sole fiocculant may be used to assist sedimentation of particles. The choice between anionic, non-ionic or cationic charge on the polyelectrolyte will depend to a large extent on the chemistry of the particles to be flocculated. Such treatment, however, will often remove only 10-30% of the COD. [Pg.161]

As discussed in Chapter 17, legislative controls including stringent consent conditions are applied in the UK to all discharges to specified sewers. (Discharge of effluent to surface water drains is prohibited.) Limits, or even total prohibitions, are placed upon certain chemicals to avoid... [Pg.505]

The consent of Woodhead Publishing Limited does not extend to copying for general distribution, for promotion, for creating new works, or for resale. Specific permission must be obtained in writing from Woodhead Publishing Limited for such copying. [Pg.528]

Research subjects may want to limit the research use of their materials and data to scientists they trust and ends of which they approve. It currently may take a lawyer s reading of the consent form to determine whether the materials and data may be shared or used for other purposes. Even if the form does limit who can use the research materials and data and for what purposes, the extent to which those forms can and will be enforced is limited. Minority groups with special concerns about the use of samples and data from their groups need to reach clear and enforceable understandings with researchers. Groups may want to limit the research use of their samples and data to the questions initially posed or further questions expressly approved by the group. Similarly, they may wish to limit to whom the samples and data can be transferred. [Pg.77]

Before a person has a genetic test, it is important that he or she understands the testing procedure, the benefits and limitations of the test, and the possible consequences of the test results. The process of educating a person about the test and obtaining permission is called informed consent. [Pg.40]

In cases in which an investigator engages in serious or continuing noncompliance, it is the responsibility of the IRB to report that activity to the sponsor and to the FDA. Noncompliance issues include, but are not limited to, unreported changes in the protocol, misuse or nonuse of fhe informed consent document, failure to submit protocols to the IRB in a timely manner, and avoiding or ignoring the IRB. [Pg.440]


See other pages where Consent limits is mentioned: [Pg.535]    [Pg.535]    [Pg.620]    [Pg.237]    [Pg.21]    [Pg.318]    [Pg.105]    [Pg.349]    [Pg.941]    [Pg.942]    [Pg.535]    [Pg.535]    [Pg.620]    [Pg.237]    [Pg.21]    [Pg.318]    [Pg.105]    [Pg.349]    [Pg.941]    [Pg.942]    [Pg.266]    [Pg.270]    [Pg.2209]    [Pg.42]    [Pg.442]    [Pg.19]    [Pg.37]    [Pg.37]    [Pg.355]    [Pg.496]    [Pg.239]    [Pg.362]    [Pg.114]    [Pg.201]    [Pg.655]    [Pg.41]    [Pg.218]    [Pg.185]    [Pg.261]    [Pg.254]    [Pg.255]    [Pg.4]    [Pg.34]    [Pg.299]   
See also in sourсe #XX -- [ Pg.21 ]




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