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制药行业在服务人类时,也带来了环境污染,所以需要建立清洁的生产模式,对污染的产生进行全过程控制。经过多年的探索和实践,清洁生产从新的质量观念出发,在其源头进行削减污染,降低消耗的理念已经被广泛认可。制药企业进行清洁生产审核要与实施GMP紧密结合起来,在对企业进行实地调研的过程中,要结合制药行业的特点,对制药企业需要关注的重点方面进行仔细盘查,分析存在的节能降耗的潜力,提出了切实有效的清洁生产方案。
When the pharmaceutical industry serves human beings, it also brings about environmental pollution. Therefore, it is necessary to establish a clean production mode and control the entire process of pollution generation. After years of exploration and practice, the concept of cleaner production at the source of reducing pollution and reducing consumption has been widely recognized, starting from the new concept of quality. Pharmaceutical companies to clean production audit and implementation of GMP closely linked to the field research in the process of enterprises, we must combine the characteristics of the pharmaceutical industry, pharmaceutical companies need to focus on aspects of careful inventory, analysis of the existing energy saving Potential, put forward a practical and effective cleaner production program.