FLIMS system strictly follows ISO 9000, ISO/IEC 17025, G(A)LP, GMP, FDA and other standards, helping enterprises to establish a complete quality assurance and quality control system, reducing operating costs and improving quality risk control, thus enabling enterprises to develop rapidly and healthily.
Standardization-Establishing Quality Management System
FLIMS system provides the quality management module of life cycle management, covering supplier management, change management, deviation management, verification management, audit management, risk assessment management, release management, complaint management, adverse reaction management, quality target management and QC management, as well as inspection management, sample retention management, stability management, personnel management and instrument management, which provides security for the quality development of enterprises. Free managers at all levels from daily GMP inspection and spend more time doing their jobs.
Controllable —— Realizing a Unified Quality Supervision Platform
The FE LIMS system monitors the whole process of raw material procurement, warehousing inspection, production process control, finished product inspection, release, complaint tracking and recall. The quality authorizer can control all quality conditions in real time through the system, put an end to all irregular quality operation processes, and take corresponding measures in the shortest time to minimize quality risks. The management process of evaluating, controlling, communicating and auditing the quality risks in the whole product life cycle by looking forward or reviewing. Through the quality risk assessment of deviation, change, verification, complaint, supplier audit and other links, the risk is minimized and controllable to ensure product quality.
Reduce consumption-save costs for enterprises
The standardized management program provided by FE LIMS system can reduce and avoid the repetition of sample preparation, thus reducing the consumption of experimental supplies such as standard materials, reagents and culture medium plates; Strictly control key materials to prevent waste; Laboratory animals are managed in a unified way, reused and targeted, and a unified quality office platform is established to realize paperless office and reduce paper waste; Statistical analysis of instrument usage to improve instrument utilization rate; Conduct quantitative assessment of personnel, optimize the allocation of human resources and reduce labor costs; Integrate the internal collaborative office platform to reduce the operating costs of enterprises.
Integration-integrating resources to improve work efficiency.
The FE LIMS system integrates the collaborative office function, which makes the quality inspection department and other departments more closely combined to form a unified quality inspection business collaborative platform. In addition to integrating internal resources, it also has good external system expansion and integration ability, that is, it supports the integration with ERP, MES, OA, HR, CRM and other systems, thus optimizing enterprise resources, reducing manual input errors and speeding up data transmission; Unify the sample registration and scheduling system, reduce the sample turnover time, increase the sample quantity, and prevent repeated sampling; Through the statistics and trend analysis of data, we can track the performance, standards and methods of products, warn the trend of poor quality changes, and prevent the generation of unqualified products, so as to achieve efficient work in the whole process of quality management.