2019年7月12日 · ISO 9000 is a family of standards for Quality Management Systems (QMS) that helps organizations provide quality goods and services while following all related laws, codes …

A Quality Management System (QMS) is defined as a set of interrelated or interacting elements such as policies, objectives, procedures, processes, and resources that are established …

2023年9月21日 · Learn what QMS documentation is, its structure, benefits, requirements, implementation process, maintenance, and the role of QMS software.

QMS系统是质量管理系统（Quality Management System）的缩写。 它是一种组织内部用于管理和控制质量相关活动的体系，旨在确保产品或服务符合质量标准和客户要求。

2019年5月31日 · We are heading into a first in human clinical trial this year and I am getting all of the kitting and labeling documentation together. I have the label created and uploaded the …

2024年7月2日 · The international standard ISO 10013:2021 Quality management systems – Guidelines for documented information gives directions for an effective QMS documentation …

2022年9月21日 · Out of ISO 9000 family, the ISO 9001 standard includes the specific requirements for creating a QMS and controlling your documents. This article will discuss the …

质量数据管理平台 (QMS)围绕生产、试验、检验各环节，通过知识图谱建立质量主数据的图数据链路，完成质量问题溯源、根因分析等业务的建设。 基于AI分析质量问题，结合质量知识库， …

2024年6月4日 · Quality control labels are the fail safe that keeps faulty or dangerous products from making it to the end of the production line and into the hands of customers, ensuring …

2024年11月12日 · Packaging and labeling play critical roles in pharmaceutical product integrity, safety, and compliance. Quality assurance (QA) measures must ensure accurate labeling, …