Academic literature on the topic 'Veterinary drug industry'

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Journal articles on the topic "Veterinary drug industry"

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Haughey, Simon A., and G. Andrew Baxter. "Biosensor Screening for Veterinary Drug Residues in Foodstuffs." Journal of AOAC INTERNATIONAL 89, no. 3 (May 1, 2006): 862–67. http://dx.doi.org/10.1093/jaoac/89.3.862.

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Abstract The advent of the surface plasmon resonance (SPR) biosensor has led to many applications in diverse fields from the pharmaceutical industry to the life sciences and other areas within biotechnology. One area that has seen a significant increase in applications is the testing for veterinary drug residues in foodstuffs. These include tests for antibiotics, β-agonists, and antiparasitic drugs. The introduction of the Biacorer<sup/>Q in the late 1990s, an SPR biosensor dedicated to the food industry, and the complementary development of kits to test for these residues mean that end users have a viable alternative screening test to the established enzyme-linked immunosorbent assay (ELISA) techniques. This paper reviews many SPR biosensor veterinary drug tests that have been developed, with particular emphasis placed on kit-based assays.
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Wang, Jianhua, Yuanyuan Deng, and Hanyu Diao. "Perceived Risk, Expected Benefits and Pig Farmers’ Behaviors of Veterinary Drug Usage." International Journal of Environmental Research and Public Health 15, no. 8 (August 10, 2018): 1716. http://dx.doi.org/10.3390/ijerph15081716.

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To guarantee the pork quality and safety and the steady development of the pig-breeding industry in China, it is important to control veterinary drugs usage in the pig farming sector. In order to develop an effective intervention that control veterinary drug usage, it is important to perform an in-depth analysis of those factors that can affect the standardized use of veterinary drugs in the pig-breeding process. In this paper, hierarchical regression analysis is used to examine how perceived risk, expected benefits, and self-efficacy influence on the standardized use of veterinary drugs. Data were collected using a multi-stage sampling method from four provinces in China. The results show that expected benefit and self-efficacy have positive impacts on the standardized use of veterinary drugs. Self-efficacy significantly moderated the positive relationships between expected benefits and the negative relationships between perceived risk and standardized use of veterinary drugs.
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Caprile, Kelli A. "Veterinary Pharmacy." Journal of Pharmacy Practice 2, no. 2 (April 1989): 83–91. http://dx.doi.org/10.1177/089719008900200205.

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Veterinary pharmacy is a specialized area of practice within the field of pharmacy as a whole. It is in the veterinary academic setting that pharmacists have established themselves as an integral and important part of the veterinary health care team in that veterinary hospital pharmacists are engaged in many different activities involving drug distribution, clinical services, teaching, and research. The average veterinary hospital pharmacy provides services that are equivalent in quality and quantity to those found in many hospitals for humans. Veterinary hospital pharmacists also play an important role as drug therapy consultants often being called upon to design dosage regimens for various types of patients. In order to be maximally effective in this setting, the veterinary pharmacist must combine knowledge of drug chemistry, pharmacology, and toxicology with an understanding of those unique anatomic, metabolic, and behavioral aspects that exist for each species of animal. Veterinary pharmacists are also often involved in clinical research with veterinary hospital clinicians and, less often, in areas of basic research with other faculty members of the veterinary school. Veterinary pharmacy is predicted to continue to grow, expand, and evolve in those areas in which it has already become established, namely, the veterinary schools and their associated teaching hospitals. There is also ample opportunity and need for pharmacists to become involved in other areas, such as the veterinary pharmaceutical industry, veterinary regulatory agencies, and agricultural and livestock production, which affect not only veterinary medicine but also public health as a whole.
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Pham, Thang Dac. "Competitive Capability of Some Typical Selected Veterinary Drug Manufacturers in Vietnam in the Context of International Economic Integration." International Journal of Human Resource Studies 11, no. 2 (April 19, 2021): 151. http://dx.doi.org/10.5296/ijhrs.v11i2.18365.

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In the process of deeper and broader integration into the world and regional economy, Vietnamese businesses in general and veterinary drug manufacturers in particular have had advantages as well as disadvantages. Veterinary medicine manufacturers’ advantages are, such as: market expansion, access to science and technology, access to capital, improving management skills, etc. Nevertheless, it also faces many challenges and risks. During the development phase, Vietnamese veterinary medicine manufacturers have to face robust competition from regional and international competitors. Besides, meeting industry standards (such as GMP) is also a prerequisite for veterinary drug manufacturers in Vietnam to focus on implementation. This study analyzes the competitiveness of Vietnamese veterinary drug manufacturers, on that basis gives discussions, thereby proposing some recommendations in order to enhance the competitiveness of Vietnamese veterinary medicine manufacturers in the context of international economic integration.
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Zvereva, Elena A., Nadezhda A. Byzova, Peter G. Sveshnikov, Anatoly V. Zherdev, and Boris B. Dzantiev. "Cut-off on demand: adjustment of the threshold level of an immunochromatographic assay for chloramphenicol." Analytical Methods 7, no. 15 (2015): 6378–84. http://dx.doi.org/10.1039/c5ay00835b.

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In this study, adjusting the threshold level was investigated for an immunochromatographic assay for chloramphenicol, which is a veterinary drug of concern in the food industry because of its toxic effects.
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Robles, Ivelisse, Andreia G. Arruda, Emma Nixon, Elizabeth Johnstone, Brooklyn Wagner, Lily Edwards-Callaway, Ronald Baynes, Johann Coetzee, and Monique Pairis-Garcia. "Producer and Veterinarian Perspectives towards Pain Management Practices in the US Cattle Industry." Animals 11, no. 1 (January 16, 2021): 209. http://dx.doi.org/10.3390/ani11010209.

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Producers and veterinarians are considered responsible for improving animal welfare, as they are responsible for implementing practices that directly impact the animal’s well-being. Most husbandry procedures performed in cattle do not include pain mitigation, and understanding challenges faced by these stakeholders to use analgesics is key in improving on-farm pain management strategies. Therefore, the objectives of this study were to explore producer and veterinarian perspectives on pain management practices by (1) exploring inquires received by Food Animal Residue Avoidance Databank (FARAD) regarding analgesic use in cattle and (2) using a survey instrument to identify factors that impact pain management implementation in the US cattle industry. Albeit analgesia use increased in the past ten years for some producers and the majority of veterinarians, administering analgesics for pain management on US cattle farms remains a challenge. From a producer perspective, drug cost, availability and logistics for administration. From a veterinarian perspective, lack of Food and Drug Administration (FDA) products hinders the support of on-farm protocols requiring extra-label drug use. Future steps to improve analgesic use on-farm include identifying and approving drugs that demonstrate efficacy for managing pain in cattle and disseminating educational resources to support stakeholders in both the implementation and drug withdrawal process.
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FRANCO, DON A., JANICE WEBB, and CLYDE E. TAYLOR. "Antibiotic and Sulfonamide Residues in Meat: Implications for Human Health." Journal of Food Protection 53, no. 2 (February 1, 1990): 178–85. http://dx.doi.org/10.4315/0362-028x-53.2.178.

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The subtherapeutic use of antimicrobial drugs has played an important role in animal husbandry by the control of disease, the improvement of growth and efficiency of feed conversion. Livestock producers, industry, veterinary, and regulatory personnel share responsibility to ensure freedom from drug metabolites, residues, and other chemicals to which livestock and poultry may be exposed. The predominant concerns are for the potential adverse effects on human health. Data demonstrate that the feeding of subtherapeutic antimicrobials to livestock and poultry increases the prevalence of R+ enteric organisms. Some of these organisms may be pathogenic for humans.
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van Tongeren, Susan, Jane A. Fagerland, Michael W. Conner, Kelly Diegel, Kevin Donnelly, Branka Grubor, Alric Lopez-Martinez, et al. "The Role of the Toxicologic Pathologist in the Biopharmaceutical Industry." International Journal of Toxicology 30, no. 5 (August 30, 2011): 568–82. http://dx.doi.org/10.1177/1091581811413304.

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Toxicologic pathologists contribute significantly to the development of new biopharmaceuticals, yet there is often a lack of awareness of this specialized role. As the members of multidisciplinary teams, toxicologic pathologists participate in all aspects of the drug development process. This review is part of an initiative by the Society of Toxicologic Pathology to educate scientists about toxicologic pathology and to attract junior scientists, veterinary students, and veterinarians into the field. We describe the role of toxicologic pathologists in identifying candidate agents, elucidating bioactive pathways, and evaluating efficacy and toxicity in preclinical animal models. Educational and specialized training requirements and the challenges of working in a global environment are discussed. The biopharmaceutical industry provides diverse, challenging, and rewarding career opportunities in toxicologic pathology. We hope that this review promotes understanding of the important role the toxicologic pathologist plays in drug development and encourages exploration of an important career option.
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Yang, Shu, Shuo Yang, Gui Juan Du, Feng Jiang Ma, and Zhe Zhang. "Discussion on the Green Products and Recycling Industry of Biotechnolongy Fulvic Aicd." Applied Mechanics and Materials 368-370 (August 2013): 486–90. http://dx.doi.org/10.4028/www.scientific.net/amm.368-370.486.

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Biotechnolongy fulvic aicd is internally-recognized green, environment-protective and natural bioactive substance. It is able to effectively solve many bottleneck problems besetting development of issues of agriculture, farmer and rural area such as rural energy, food safety, environmental pollution, agricultural high yield and efficiency and agricultural sustainable development through developing BFA technology and its industry and developing methane, compound fertilizer, pesticide, growth regulator, feed additives and veterinary drug etc. by use of husbandry, industrial by-product and organic household refuse as raw materials to realize cyclic utilization of substance.
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Kitandu, A., and R. Juranová. "Progress in Control Measures for Chicken Coccidiosis." Acta Veterinaria Brno 75, no. 2 (2006): 265–76. http://dx.doi.org/10.2754/avb200675020265.

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For many years, prophylactic use of anticoccidial drugs has been the primary means of controlling chicken coccidiosis in broiler industry and has played a major role in the growth of this industry. Also the use of live vaccines is well established in the control of the disease. Three groups of live vaccines can be distinguished based on the characteristics of the Eimeria species included in the product: vaccines based on live virulent strains, vaccines based on live attenuated strains, vaccines based on live strains that are relatively tolerant to the ionophores, and non-live subunit vaccines. The mounting problem of drug resitance of Eimeria species has prompted major research efforts to seek alternative means of control through increased knowledge of understanding the immunomodulation, natural-product feed additives, advances in live and recombinant vaccines. This article reviews the above mentioned methods in control of chicken coccidiosis.
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Dissertations / Theses on the topic "Veterinary drug industry"

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Luangtongkum, Taradon. "Campylobacter spp. in conventional and organic poultry operations." Connect to resource, 2005. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1123790867.

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Thesis (Ph. D.)--Ohio State University, 2005.
Title from first page of PDF file. Document formatted into pages; contains xii, 304 p.; also includes graphics. Includes bibliographical references (p. 253-304). Available online via OhioLINK's ETD Center
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Books on the topic "Veterinary drug industry"

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Gathuma, Joseph M. Comparative analysis of veterinary drugs delivery mechanisms in the arid lands of Kenya. Nairobi, Kenya: Agricultural Research Foundation, 2004.

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Kyōkai, Nihon Dōbutsuyō Iyakuhin. Dōbutsu yakuji kankei kijun kaisetsushoshū: GQP, GVP, GMP, kōzō setsubi kisoku, GCP, GPSP no kaisetsu (kankei kijun no kakujō kaisetsu to Q & A, tejunsho moderu). Tōkyō: Nihon Dōbutsuyō Iyakuhin Kyōkai, 2008.

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Animal Drug User Fee Act of 2003: Report (to accompany S. 313). [Washington, D.C: U.S. G.P.O., 2003.

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4

Santon, June. Animal health care products. Norwalk, CT: Business Communications Co., 1997.

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Animal Drug User Fee Act of 2003: Report (to accompany H.R. 1260) (including cost estimate of the Congressional Budget Office). [Washington, D.C: U.S. G.P.O., 2003.

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Miller, Richard Kendall. Survey on biotechnology in animal agriculture. Madison, GA: Future Technology Surveys, 1989.

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Animal Health Companies Association of Bangladesh. Membership directory, 2013. Edited by Islam, M. Nazrul (Businessman), editor. 4th ed. Dhaka: Animal Health Companies Association of Bangladesh, 2013.

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Conference on International Harmonisation of Veterinary Medicinal Products (1st 1999 Brussels, Belgium). First Conference on International Harmonisation of Veterinary Medicinal Products, 16-18 November 1999--Brussels, Belgium: VICH 1. Luxembourg: Office for Official Publications of the European Communities, 2000.

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Office, General Accounting. Food safety and quality: FDA strategy needed to address animal drug residues in milk : report to the chairman, Human Resources and Intergovernmental Relations Subcommittee, Committee on Government Operations, House of Representatives. Washington, D.C: The Office, 1992.

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Office, General Accounting. Food safety and quality: Innovative strategies may be needed to regulate new food technologies : report to the Chairman, Subcommittee on Oversight and Investigations, Committee on Energy and Commerce, House of Representatives. Washington, D.C: The Office, 1993.

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Book chapters on the topic "Veterinary drug industry"

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Hagren, V., P. Peippo, and T. Lovgren. "Detecting and controlling veterinary drug residues in poultry." In Food Safety Control in the Poultry Industry, 44–82. Elsevier, 2005. http://dx.doi.org/10.1533/9781845690236.44.

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