- An effective pharmaceutical quality management system (QMS) will help you develop a culture of quality, support data integrity, keep suppliers under control, and maintain overall compliance. QMS data must also be structured to drive consistent metrics, risk calculations, and other trend analysis.
- A QMS system is the crux of any quality and compliance process. It is a regulatory requirement that Food and Drug Administrator regulatory inspectors and ISO auditors consider critical.
- TPS company help the pharmaceutical industry to build or reorganize quality management systems (QMSs).
QUALITY MANAGEMENT SYSTEM
Quality Management System
QMS in Production
TPS company help to propose an ideal SOP documentation structure based on quality assurance policies. The service also covers documentation support, including batch records (BRs) for making a reliable and efficient release, and SOPs and other records for assuring high-quality manufacturing operations.
QMS in Equipment and Facilities
TPS company will review clients’ facility layouts, cleanliness zoning, and flow of personnel and materials to propose measures for improvement.
TPS company provides the service which covers support for the drafting of Validation Master Plans (VMP- Validation documentation Service) and other related documents based on the risk-based analysis, and guidance for implementing DQ/IQ/OQ (design qualification, installation qualification, and operational qualification) including review and guidance for execution and record keeping.
QMS in Laboratory Control
TPS company covers support for building a wide range of quality assurance systems, including management of samples/reference standards/reagents, validation of analytical methods, and qualification/maintenance/calibration of test equipment.
QMS in Materials
TPS company will propose appropriate methods to control warehousing and loading/unloading of materials and products.