ASSESSMENT OF PRODUCTION AND TECHNOLOGICAL RISKS IN THE ACTIVITIES OF VETMEDICINE ENTERPRISES

V. Velychko, A. Grymak, L. V. Kurylas, T. Y. Seneshyna
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Abstract

Risk is the possibility of a negative discrepancy and the likely scale of its consequences over a period of time. Giving producers of products for veterinary medicine and animal husbandry (such as veterinary drugs, protective equipment, feed, feed additives, etc.) responsibility for the production of quality products obliges them to clearly and systematically control all hazards that may occur in the production. The essence of effective product quality control is to ensure that measures to produce quality products are adequate and meet the task - not to harm animals and birds, provided the correct way of their use, as well as people. Accordingly, all production processes must be clearly regulated and periodically reviewed in the light of experience and the situation on the product market. Systematic control of the stability of production for veterinary medicine and animal husbandry according to the parameters defined in the quality specification is justified. It should be borne in mind that the activities of enterprises may be influenced by factors that hinder the implementation of the goals. G. Verbytska (2004) notes that the existing theory of both quantitative and qualitative risk assessment requires relevant information, although the information market on these issues is still underdeveloped. Therefore, the target methods of quantitative risk analysis are not developed, and the existing ones are not universal. Therefore, there is a need to combine methods, or their individual elements. Analysis of dangerous factors is always specific to each process and production as a whole, so it cannot be "borrowed" from another manufacturer, even if it produces similar products. The experience of leading domestic and foreign veterinary companies shows that the analysis of dangerous facts (risks) consists of a series of consistent, logically interrelated actions. The risk factors of the manufacturer should be considered as those under the direct influence of management. Therefore, their identification, analysis results, development of measures to minimize risks are considered one of the priority tasks of enterprise management, which is carried out by its management. Analysis of the activities of a number of enterprises, in particular the results of monitoring and selective control of product quality, confirms that there is a significant level of risk for veterinary enterprises. Their timely assessment and prompt application of appropriate measures can neutralize the identified risks, or eliminate the possibility of their occurrence Chornyi (2017). Inability or untimely assessment of risks excludes the possibility of their control. Therefore, the study of industrial and technological risks are relevant, and their timely detection warns of various threats and economic security of enterprises. Risk assessment of veterinary enterprises in modern conditions is unresolved, not specified in the methodological support of their assessment, which determines the importance of such studies.
兽药企业经营活动中的生产和技术风险评价
风险是在一段时间内出现负差异的可能性及其后果的可能程度。赋予兽药、畜牧业产品(如兽药、防护装备、饲料、饲料添加剂等)生产者生产优质产品的责任,使其有义务对生产中可能发生的一切危害进行清晰、系统的控制。有效的产品质量控制的本质是确保生产优质产品的措施是充分的,并满足任务-不伤害动物和鸟类,提供正确的使用方式,以及人。因此,必须根据经验和产品市场情况对所有生产过程进行明确管理和定期审查。根据质量规范中规定的参数对兽药和畜牧业生产的稳定性进行系统控制是合理的。应当铭记,企业的活动可能受到妨碍实现目标的因素的影响。G. Verbytska(2004)指出,现有的定量和定性风险评估理论都需要相关信息,但这些问题的信息市场尚不发达。因此,定量风险分析的目标方法尚未开发,现有的方法也不具有普遍性。因此,有必要将方法或它们各自的元素组合起来。危险因素的分析总是具体到每一个过程和生产作为一个整体,所以它不能“借用”从另一个制造商,即使它生产类似的产品。国内外领先的兽医公司的经验表明,危险事实(风险)的分析由一系列一致的、逻辑上相互关联的行动组成。制造商的风险因素应视为受管理层直接影响的因素。因此,它们的识别、分析结果、制定措施以降低风险被认为是企业管理的首要任务之一,这是由其管理层进行的。对一些企业活动的分析,特别是对产品质量的监测和选择性控制结果的分析,证实了兽医企业存在显著的风险。及时评估并及时采取适当措施可以消除已识别的风险,或消除其发生的可能性(Chornyi(2017))。不能或不及时的风险评估排除了控制风险的可能性。因此,对产业和技术风险的研究是有意义的,对它们的及时发现为企业的各种威胁和经济安全提供预警。兽医企业在现代条件下的风险评估尚未解决,在评估的方法支持中没有具体说明,这决定了此类研究的重要性。
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