FE LIMS

タイトルまたは説明

Zhuhai Feiqi Software Co., Ltd. in the face of opportunities and challenges, with thedomestic famous enterprises (Livzon pharmaceutical) years very fruitful cooperation,forge ahead and follow a new version of the GMP total quality management on the requirements of pharmaceutical enterprises, the grand launch of information management software *- the pharmaceutical quality control system can meet the requirement of construction of the ***0 edition of the GMP quality system (FELIMS),quality control and quality assurance as the core, centralized control of productionand material management, provide the most information and objective, timely,accurate, reliable product quality control parameters for the key person in charge ofenterprises, help enterprises to reduce costs, life cycle management of drugs.

The pharmaceutical quality control system (FELIMS) distributed system consisting ofan open, for the realization of laboratory management, improve the overall level of risk assessment and management, file management system, product quality review,production management, materials management, equipment management, informationintegration and sharing, cost control, instrument and automatic data collection and other aspects provide technical support at the same time, also can meet the needs of the construction of quality management system requirements, staff performancemanagement and OA office.

The pharmaceutical quality control system (FELIMS) to help enterprises on the basis of the ***0 version of the GMP specification requirements, ensure that enterpriseshave a good production equipment, a reasonable production process, improve the quality of management and strict inspection system, so that the final product quality in compliance with regulatory requirements.

Following the ***4 implementation of GMP caused the pharmaceutical industryreshuffle, the GMP also launched a new round of industry reshuffle, how to remain invincible in the crisis, pharmaceutical quality control system (FELIMS) to help youimprove the quality system, and enterprise together, smoothly through the new version of GMP.