Zhejiang Asia-Pacific Pharmaceutical Co., Ltd. tablet layout Process Improvement Workshop smoothly through spot checks

Zhejiang Asia-Pacific Pharmaceutical Co., Ltd. tablet layout Process Improvement Workshop smoothly through spot checks recently, Shaoxing City by the Food and Drug Authority in the EAA commissioned by the Food and Drug Pharmaceutical Co., Ltd. of Zhejiang Asia-Pacific workshop tablet layout process for improving the situation the spot checks. The workshop examined the original tablets in June 2002 through the national GMP certification, the main production tablet, capsule. Due to business expansion, enterprise development needs, from the Asia-Pacific medicine this year in July, its technology, and improved layout, and new intermediate stations and the 71 m2 clean zone. Inspection teams should act in line with the "pharmaceutical production and quality control" requirement, and after adjustment for additional equipment, such as air purification system conducted a comprehensive detailed inspection and found no serious flaws in the layout of the view that the workshop improved more reasonable, in line with Evaluation Standards certification inspection