QMS documentation discussed in this article are documents and records related to compliance and quality assurance. These documents define the company’s Quality Management System (QMS). The QMS documentation is defined by each company based on regulatory and...
A Laboratory Quality Management System (LQMS) refers to a set of policies, procedures, and practices implemented in a laboratory to ensure consistent quality and accuracy in its operations. Various standards and regulations outline specific requirements for...
What Is an eQMS? An eQMS is an Electronic Quality Management System that helps businesses automate and streamline their quality management processes. With eQMS, quality teams can manage and track quality management-related activities, such as document control, change...
A Medical Device Quality Management System (QMS) is a set of policies, processes, and procedures that a manufacturer of medical devices has in place to ensure that their products are safe and effective for their intended use. The QMS includes all aspects of design and...
Pharmaceutical Quality Management System (QMS) is a set of procedures and practices contributing to product quality. The QMS must reflect the relevant regulatory requirements applicable to the industry and company. In the pharmaceutical industry, some of the important...
An effective quality management system (QMS) is a system that enables a company to consistently provide products and services that meet customer and regulatory requirements. Effective quality management has become a necessity in the Life Science industry. A...
