GMP Software for Quality in the Pharmaceutical Industry The interplay between quality and safety is particularly important in the pharmaceuticals industry, as very often lives rely directly on the products that are developed and produced. That is why this sector is closely monitored by various authorities, who ensure that nothing is brought to market that does not comply with pertinent quality and safety measures and that the product, production process, packaging, and shipping are all faultless. It comes as no surprise, that adherence to their quality standards and compliance guidelines are make-or-break factors for any company operating in this sector. Document Management Software QBD.Net Quality Management Software Solutions Due to these demands, the companies rely on production practices such as the so-called Good Manufacturing Practice (GMP). This is a set of guidelines that provides guidance for manufacturing, testing, and quality assurance in order to ensure that a manufactured product is safe for human consumption or use. Properly maintaining the associated tools, however, is difficult with pen and paper or spreadsheet solutions alone. This is where the CAQ.Net software solutions come into play. They facilitate the targeted implementation of individual software modules in order to create a scalable, future-proof, and fully integrated quality management and LIMS system that is validatable in accordance with Good Automated Manufacturing Practice (GAMP) guidelines. Most Popular Components of the GMP Software Document ControlDocument relevant control steps at any time and enable all employees to access all the documents they need in the current and valid version at the right time.Learn more about the Document Control Software » Change ControlKeep track of all details at all times by centrally monitoring and controlling all change processes in your company.Learn more about the Change Management Software » CAPANo matter in which area the trigger for a Corrective and Preventive Action lies - with CAQ.Nets assistant-based functions you can initiate a CAPA process from within gauge management, audit management, or complaint processing and perform necessary actions across all modules.Learn more about the CAPA Assistant » Risk ManagementIdentify, evaluate, and document relevant risks in order to meet the requirements of Good Manufacturing Practice.Learn more about the Risk Management Software » Root Cause AnalysisUncover potential for improvement and explore the root causes of problems by applying Ishikawa diagrams and the 5-Why method.Learn more about the RCA software » Skills MatrixInstantly ascertain which employees need which qualifications, which qualifications they hold, and which qualifications need to be renewed.Learn more about the Skills Matrix Software » Data ValidationSeamlessly document and track all data changes in your CAQ system.Learn more about the Audit Trail Function in CAQ.Net » LIMSHolistic sample management supports you throughout all analyses, inspections, and examinations in the laboratory.Learn more about the LIMS Software » More ComponentsLearn more about Quality Management Software » Pharmaceutical Companies that Rely on CAQ.Net