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Novartis adopted its first global Code of Conduct in 1999. In order to reflect the signing of the Global Compact in 2000, an amendment became necessary. The revised version of our Code of Conduct was distributed in 2001 to all Novartis Group company employees worldwide and translated into local languages. Compliance with our Code of Conduct, which is a part of the employment terms of all Novartis employees is closely monitored. For this we have established a worldwide network of over 45 Compliance Officers who advise on compliance problems, deal with complaints and handle any arising issues. Their reports are consolidated by the Group Compliance Officer into a yearly Compliance Report addressed to the Audit and Compliance Committee of the Board. Issues and Problems As might be expected for a Group with more than 70 000 associates, Novartis had its share of issues and problems to deal with in 2002. Reported cases related particularly to discrimination and harassment, conflicts of interest, inappropriate marketing practices and some inappropriate payments. Sanctions resulting from such infringements included 18 dismissals. Code of Conduct Survey Results This annual survey, conducted this year with more than 3 500 associates, provided additional insight into the acceptance of the Code. The results show that there is a high awareness of the Code. More than 80% of the respondents felt adequately or very familiar with the contents of the document. More than half, however, felt that they lacked sufficient training regarding the detailed implementation in their daily work of the principles laid out in the Code. Outlook The key findings of both the compliance reports and the surveys are that the Code is very well accepted and its principles are considered as the appropriate way to behave and to conduct business. Reports and comments range from "established and absolutely uncontested" in a Scandinavian country to "an excellent initiative since the government has just launched a mega action against corruption" in an African country. All in all, Novartis is essentially compliant with the Code, but it will require constant management attention in all critical fields and countries to maintain this status. In 2003, we will focus on the needs for action shown in the surveys and in the reports. New training tools will be created and training programs for associates have already been launched. Professional training of the members of the compliance organization will be intensified. The main challenge will be to continue creating an open climate of discussion and reporting, thereby ensuring that problems and cases can be discussed and reported without fear of retaliation. Another planned activity relates to the complaints procedure, the right of all associates to complain to the Compliance Organization about violations of the Code of Conduct. Experience has shown that the awareness of the existence of such procedures diminishes over time and suitable activities will be taken to ensure that associates are regulary reminded of its existence and terbutaline.
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Stances, the federal law preempts state unfair competition claims. Answering both questions in the negative, the Court affirmed a district court's judgment denying a motion to dismiss based on such claims. Elo Touch Systems, Inc. "Elo Touch" ; sued Exzec, Inc. "Exzec" ; for infringement of patents directed to touch panel systems for computers. In response, Exzec asserted two counterclaims against Elo Touch for unfair competition, one under 43 a ; of the Lanham Act, 15 U.S.C. 1125 a ; , and the other under Illinois common law. Elo Touch supported its claims of unfair competition by alleging that Elo Touch had known or should have known that Exzec's touch panels used shear technology while Elo Touch's patents were limited to touch panels that use surface acoustic wave technology, and therefore, Exzec did not infringe Elo Touch's patents. Exzec further alleged that despite this knowledge, Elo Touch falsely had told potential customers that Exzec's touch panel infringed its patents and that Exzec could not manufacture or sell a noninfringing acoustic touch panel system. In ruling on a motion to dismiss, the district court noted that while allegedly false representations of patent infringement are generally not actionable under 43 a ; , allegedly false representations that the patentee is the exclusive source of a certain type of product because of its patent may be actionable under 43 a ; . The district court therefore denied the motion to dismiss, focusing on the Exzec's allegation that Elo Touch told potential customers that Exzec could not manufacture a device that would not infringe its patents. On appeal, the Federal Circuit ruled that Exzec's 43 a ; claim was not barred by federal antitrust laws. The Court also found that the antitrust laws and the Lanham Act have a common purpose of fostering fair competition, while the elements of a federal antitrust claim and a 43 a ; claim are substantially different e.g., antitrust claims require establishment of a monopoly power ; . The Court held that recognizing a 43 a ; claim in this context would not thwart the congressional purpose embodied in the antitrust laws. The Court then turned to whether Exzec's 43 a ; claim was barred by the patent laws. The Court found that the antitrust and patent laws were complementary in purpose as they each promoted innovation and competition, but that a conflict seemingly arose when an accused infringer attempted to use antitrust laws to frustrate a patentee's right to enforce a patent. The solution to this conflict has been to block antitrust suits against patentees attempting to enforce its patent. However this barrier is lifted in the case where an antitrust counterclaim is based on the patentee allegedly and baclofen.
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Insurance coverage for our directors and officers, which could make it difficult to attract or retain qualified directors and officers. We are at an early stage of development. We are at an early stage of development. Our drug candidate cannabinor has completed Phase I testing and is scheduled for preliminary proof-of-principle Phase IIa testing in various pain indications during the first half of 2006. Apart from an ophthalmic product that was sold to Bausch & Lomb Incorporated in October 2001, in which we have a financial interest, most of our other potential products are early in the research and development phase, and product revenues may not be realized from the sale of any such products for at least the next several years, if at all. Many of our proposed products will require significant additional research and development efforts prior to any commercial use, including extensive preclinical and clinical testing, as well as lengthy regulatory approval. Because of the uncertain nature of the process, we cannot be sure that our research and development efforts will be successful, that our potential products will prove to be safe and effective in clinical trials or that we will develop any other commercially successful products. We have a history of operating losses and expect to sustain losses in the future. We have experienced significant operating losses since our inception. As of December 31, 2005, we had an accumulated deficit of approximately 5.9 million. We expect to incur operating losses over the next several years as our research and development efforts and preclinical and clinical testing activities continue. Our ability to generate revenues and achieve profitability depends in part upon our ability, alone or with others, to successfully complete development of our proposed products, to obtain required regulatory approvals and to manufacture and market our products. We may not be able to obtain financing in the future. As of December 31, 2005, we had an accumulated deficit of approximately 5.9 million. The development of our technology and potential products will require a commitment of substantial funds to conduct the costly and timeconsuming research necessary to develop and optimize our technology, and ultimately, to establish manufacturing and marketing capabilities. Our future capital requirements will depend on many factors, including: continued scientific progress in the research and development of our technology and drug programs; our ability to establish and maintain collaborative arrangements with others for drug development; progress with preclinical and clinical trials; the time and costs involved in obtaining regulatory approvals; the costs involved in preparing, filing, prosecuting, maintaining and enforcing patent claims; competing technological and market developments; changes in our existing research relationships; and effective product commercialization activities and arrangements.
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1 Department of Clinical Pharmacology, 2 Division of Endocrinology and Metabolism, Department of Internal Medicine III, 3 Department of Surgery, Medical University of Vienna 4 1. Medical Department of Internal Medicine, Hanusch Hospital, Vienna; Austria.
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NOTES TO THE NOVARTIS GROUP CONSOLIDATED FINANCIAL STATEMENTS Continued ; 21. Other short-term liabilities Continued ; In May 2001, charges of CHF 21 million were incurred in relation to the closure of the Consumer Health production facility in Kings Langley, UK. The charges comprised employee termination costs of CHF 19 million and other third party costs of CHF 2 million. 250 employees were identified in the original plan, all of whom have left the Group as of December 31, 2002. In October 2002, charges of CHF 30 million were incurred in conjunction with the divestment of the Food & Beverage business to Associated British Foods plc ABF ; . The charges comprised employee termination costs of CHF 14 million and other third party costs of CHF 16 million. Originally 933 associates were identified as assigned to this business, of whom 866 were able to transfer to ABF. Natural attrition and internal redeployment limited necessary job losses to 45, of whom 42 remained employed by the Group as at December 31, 2002, but all of whom are expected to leave in 2003. All significant actions associated with the plan are expected to be completed during 2003. In December 2002, provision was made for charges of CHF 40 million in conjunction with the plan to re-organize the Health Food and Slimming and Sports Nutrition businesses into a stand-alone unit called Nutrition & Sant. The charges comprised employee termination costs of CHF 26 million and other third e party costs of CHF 14 million. It is expected that 120 job losses will result in 2003. All actions will be completed during 2003 and 2004. In December 2002 charges of CHF 14 million were incurred in conjunction with the plan to restructure the OTC business. The charges comprised employee termination costs of CHF 12 million and other third party costs of CHF 2 million. It is expected that approximately 90 positions would be impacted by the restructuring, which is planned to be completed during 2003. The releases to income in 2002, 2001 and 2000 of CHF 36 million, CHF 18 million and CHF 39 million respectively were mainly due to settlement of liabilities at lower amounts than originally anticipated. Tangible fixed asset impairments are determined based on the review of the carrying values of tangible fixed assets. Write-downs are recorded for tangible fixed assets impaired or related to activities to be restructured, divested or abandoned. The provision is transferred to accumulated depreciation as the tangible fixed assets are restructured, divested or abandoned. Other third party costs are mainly associated with lease and other obligations due to the abandonment of certain facilities. In 2002, there were no 2001: CHF 30 million, 2000: CHF 7 million ; tangible fixed asset impairments relating to restructuring which were charged directly to the income statement without being recorded in the restructuring provision and urecholine.
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Official documentation of 501 c ; 3 ; status is limited to documentation from the Federal Internal Revenue Service IRS ; . Letters from the State, attorneys, accountants, and or CPAs are not acceptable. No more than 10% of the aggregate amount allocated for services may be used for provider administrative expenses. Administrative costs are those agency expenses related to administrative costs and overhead e.g., data entry clerks, secretaries, etc. ; as opposed to those costs associated with the provision of direct services for Persons Living with HIV disease. V. LOCAL POLICIES AFFECTING FUNDING.
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We need your help as soon as possible. WE DO NOT HAVE ENOUGH ITEMS TO HOLD THE YARD SALE! The two yard sales a year are the most profitable fundraisers we do each year. HPS counts on that income to provide springtime needs. Please look around the attic and basement for items you can donate for the sale. Anything in your house, attic, basement, garage or storage buildings you don't need. We do! If we have already cleaned out your house, please ask your neighbors and friends for their unwanted items. Please round up your things and if you can't bring them to the sanctuary we will arrange pick up. Thank you for caring.
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HCPCs Generic Name Brand Name * Basis for Code Decision J2930 Injection, Solu-Medrol, A-methaPred D methylprednisolone sodium succinate, up to 125 mg J2940 Injection, somatrem, 1mg Protropin B J2941 Injection, somatropin, 1mg Humatrope, Genotropin, B Nutropin J2950 Injection, promazine HCI, Sparine, Prozine-50 D up to 25 mg J2993 Injection, retaplase, 18.1 mg Retavase D J2995 Injection, streptokinase, per Streptase D 250, 000 IU J2997 Injection, alteplase Activase D recombinant, 1 mg J3000 Injection, streptomycin, up Streptomycin Sulfate D to 1 J3010 Injection, fentanyl citrate, Sublimaze D 0.1 mg J3030 Injection, sumatriptan Imitrex A succinate, 6 mg J3070 Injection, pentazocine, 30 Talwin D mg J3100 Injection, tenecteplase, 50 TNKase D mg J3105 Injection, terbutaline sulfate, Brethine, Bricanyl D up to mg Subcutaneous J3120 Injection, testosterone Delatestryl A, B enanthate, up to 100 mg J3130 Injection, testosterone Delatestryl A enanthate, up to 200 mg J3140 Injection, testosterone A suspension, up to 50 mg J3150 Injection, testosterone A propionate, up to 100 mg J3230 Injection, chlorpromazine Thorazine D HCI, up to 50 mg J3240 Injection, thyrotropin alpha, Thyrogen D 0.9 mg, provided in 1.1 mg vial J3245 Injection, tirofiban HCI, Aggrastat D 12.5 mg J3250 Injection, Tigan D trimethobenzamide HCI, up to 200 mg J3260 Injection, tobramycin Nebcin D sulfate, up to 80 mg J3265 Injection, torsemide, 10 Demadex D mg ml J3280 Injection, thiethylperazine Torecan D maleate, up to 10 mg J3301 Injection, triamcinolone Kenalog-10, Kenalog-40, D acetonide, per 10 mg Triam-A and terbutaline.
Width, super elevation, design vehicle, minimum vertical clearance, level of service, functional street classification, and traffic volumes. Traffic volumes shall be determined for the current year, and for twenty years from the proposed construction year. These projections shall consider current and future land use. Design speed for the project shall be the current posted speed limit plus 10 miles per hour, unless otherwise approved by the District. After design speed is selected, the required stopping sight distance, vertical alignment widths, maximum grades and clear zone can be determined. Existing conditions need to be reviewed to determine the horizontal alignment. The Level of Service for District projects shall be a minimum of "C." In some cases, the cost of construction for the recommended level of service becomes prohibitive. Then, a lower level of service may be acceptable for economic or property impact reasons. Justification for the reduced level of service must be documented and approved by the District. The District has adopted the AASHTO publication "A Policy on Geometric Design of Highways and Streets", latest edition. This must be used for new and reconstruction projects on roadway systems. It is a District policy that all design criteria will be met. Where both minimum and desirable values are provided, every reasonable effort shall be made to achieve the desirable standards. The roadway widths adopted by the District shall be used. If the proposed width or other standard is less than the AASHTO standards, it must be documented, justified and approved by the District. In addition to the AASHTO Geometric Design Standards, the AASHTO Roadside Design Guide shall be used in the concept analysis and actual project design. 3105.3 Environmental Evaluation Environmental documentation starts with the concept or initial step of project development. This documentation must use existing studies pertaining to social, economic and environmental impacts of the project activities. Preliminary engineering, surveys, soil surveys, and location decision documentation can be completed before or at the same time as the environmental evaluation document Exhibit 4 ; . All interested parties, agencies or jurisdictions must be identified and involved early in the environmental process. The governmental agencies shall be involved in data collection, impact assessment and identification of such issues as bikeways, wetlands, landscaping, and noise mitigation, when appropriate. Decision making will be in the best interest of the public. Environmental documentation for a project may be governed by the following materials. 1. National Environmental Policy Act NEPA ; of 1969; 2. "Council on Environmental Quality Regulations for Implementing NEPA" 40 CFR Parts 1500-1508, November 29, 1978.
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