Administrative Issues

Conduct a review that evaluates if the equipment is appropriate for the specific lifting or moving activity. The review should involve onsite testing of a variety of equipment by the end users. Provide for the convenient storage of assist and institutional equipment. This can ensure that equipment is easy to find and, in turn, help encourage healthcare workers to use it Use flexible purchasing procedures that allow for the evaluation and purchase of up-to-date equipment with the most appropriate features. Administrative issues affect the equipment available to anployees, the types of work tasks they perform, and the methods of accomplishment. 

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Waiver of in vivo bioavailability and bioequivalence studies for immediate release solid oral dosage forms based on a biopharmaceutics classification system. Center for Drug Evaluation and Research, Food and Drug Administration, issued 8/2000, posted 8/31/2000. http //www.fda.gov/cder/guidance/ index, htm... 

The SVE case history discussed is included as a typical situation, similar to many projects encountered in the field that diverge from the ideal case. The site is located adjacent to a vehicle maintenance building in southern California. A 3000-gal and a 5000-gal UST were used to store unleaded gasoline, and a 550-gal UST was used to store petroleum-based paint thinner (Figure 10.15). To add to the situation, different phases of the project were completed by different consultants, and, due to administrative issues, almost 4 years passed between removal of the USTs and completion of the remediation activities. 

Health and Safety Guides (HSGs) (see Figure 2.3) provide concise information in nontechnical language, for decision-makers on risks from exposure to chemicals, together with practical advice on medical and administrative issues. 

Different warnings to clinicians have been issued on the link between atypical neuroleptic drugs and cerebrovascular adverse events. The US Food and Drug Administration issued a similar warning in April 2003 (595). These warnings have led to a controversy among doctors (596,597). 

The coordination structure already established in the first funding period deals with administrative issues on different levels Firstly, the activities within the HBPP are managed by the coordination team. Furthermore, the crossbridging to the... 

Creation of U.S. Medicare and Medicaid Programs Medicare Stimulated the growth of hospital pharmacy positions Medicaid Created demand for millions of prescriptions Created administrative issues Created prepaid third-party prescription payment systems... 

The United States Food and Drug Administration issued a safety alert in 1994 regarding the potentially life-threatening formation of precipitates in parenteral nutrition admixtures (148). They had received reports of two deaths and at least two cases of respiratory distress during intravenous infusion of a three-in-one parenteral nutrition mixture (amino acids, carbohydrates, lipids). The mixture contained 10% FreAmine III (amino acids -I- magnesium acetate -I- phosphoric acid -I- potassium chloride -I- sodium acetate -I- sodium chloride), dextrose, calcium gluconate, potassium phosphate, other minerals, and a lipid emulsion. The solution may have contained a precipitate of calcium phosphate. Autopsies revealed diffuse microvascular pulmonary emboli containing calcium phosphate. 

Many importing countries require proof of registration of medicinal products in the country of origin before sales are permitted. To assist local manufacturers with export markets, the National Pharmaceutical Administration issues Certificates for Exporter of Medicinal Products to holders of product licences whose locally manufactured products conform to required standards of quality (See Appendix 7). The WHO format is used. 

A total of 503 interventions were reported clinical consultations, correction of prescribing eiTors, and patient treatment procedures accounted for approximately two-thirds of the interventions (Table 6). In this study, all clinical interventions were related to chemotherapy-related toxicides or drug-dosing and -administration issues. The 167 documented clinical consultations were related to nausea or vomiting (29.3%), chemotherapy dosing or... 

Stability Testing of Drug Substances and Drug Products (Draft Guidelines), Food and Drug Administration, issued June 1998. 

The initiative has motivated a broad shift in focus for the Laboratory 8 system design and production work. Whereas prior projects were undertaken to support the EPA efforts to review permit applications for hazardous waste land disposal sites future systems will address needs in the implementation and management of clean up activities at Superfund sites. New systems will also address a more encompassing range of issues than previous systems. In addition to issues of parochial interest to the Laboratory advice about legal, regulatory, and administrative issues is to be provided. 

Facilitating administrative issues for entering assisting teams equipments to requesting state parties -RSP- (needs some special rules in all state parties or bilateral agreement). 

The Baking Division of the U. S. Food Administration issued the following ruling in 1918 Due to short supply of wheat flour, substitutes must be UBed in all bakery products beginning April 14, 19.18, as follows ... 

II) the Administrator issues such an order respecting such substance but such order does not take effect because objections were filed under paragraph (I)(C) with respect to it, the Administrator, through attorneys of the Environmental Protection Agency, shall apply to the United States District Court for the District of Columbia or the United States district court for the judicial district in which the manufacturer or processor, as the case may be, of such substance is found, resides, or transacts business for an injunction to prohibit or limit the manufacture, processing, distribution in commerce, use, or disposal of such substance (or to prohibit or limit any combination of such activities). 

D) If the Administrator issues an order pursuant to subparagraph (A) (i) respecting a chemical substance and objections are filed in accordance with subsection (e)... 

The hazards identification process must include a review of previous incidents and those near misses which had the potential to create a serious accident. The OSHA standard also identifies administrative issues (such as operating procedures and training) as being an important part of a hazards analysis. In addition, the standard calls for an analysis of siting and human factors. 

Also, all related elements of process safety (Tables 1.1 and 1.2), such as operating procedures, P IDs, training, and asset integrity, must be updated. All these items fall under the area of Process Safety Information. It is vital that all process safety information be updated before the change is actually made otherwise, there is a good chance that these administrative issues will be deferred indefinitely. 

In 1974, the project administrator issued a draft original environmental impact statement (DOEIS) for the first scaled-down project. In response to extensive public hearings and mixed reactions to the first version from about 400 special interest groups, the project was further downsized - to 181 acres and 7100 apartments. The second scaled-down version was dubbed Westway, in hopes of distinguishing it from the earlier, more vociferously opposed versions of the project. ... 

December 2001 The Ministry of Work and Administration issues the white paper, About health, environment and safety in the petroleum sector , St.meld. nr. 7 (2001-2002)... 

On 3 July 2000, two members of the parliament presented a proposal that the government should issue a white paper on HSE conditions on the Norwegian continental shelf (Dokument nr. 8 90 1999-2000). The Ministry of Labour and Government Administration issued a new white paper on health, environment and safety in the petroleum activities on 14 December 2001 (St.meld. nr. 7 2001-2002). This white paper signalled a higher ambition level than the previous one ... 

Safety and Health Program Management Guidelines. Occupational Safety and Health Administration. Issued at 54 Federal Register 3904, January 26, 1989. 

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