CAPA Management Software - Qualityze

With the help of CAPA management software system, you can attain valuable insights into the quality problems and also the possible risks. It helps to sustain the regulatory compliance for your business. With this Qualitze CAPA Management Software, you can use the Investigation task to document the investigation result or outcome. This Investigation task is where you document the root cause and perform the risk assessment. The flexibility feature of this software allows you to document multiple root causes and also the documents the results of investigation.

CAPA software is generally used by any business which makes the use of a quality control system. This CAPA software is majorly used by the manufacturers who needs to ensure that their processes and products successfully meet the regulatory ethics of their industry. This CAPA management software system is an essence of any quality and compliance process. Qualityze CAPA system helps in reducing the audit time and findings and also decreases the risk of product recalls. Qualityze CAPA management software is one of the foremost cloud-based CAPA software in field of life science, manufacturing, automotive, healthcare, medical device, pharmaceuticals and other industries.

CAPA management software of Qualityze comes up with a successful feature that includes Centralized CAPA Database, Audit Trail, Risk Matrix, Personalized Dashboards, Task Scheduler

E-Signature Validation, Chatter, and more. Qualityze has the flexibility feature which helps and allows you to treat the most important part of the CAPA management system. This software does the root cause analysis in an efficient manner which helps you to make the right decision all the time. This software supports you with the planning through its resolution step and helps to get an initial risk assessment for planning the course and the level of investigation. There is not necessary that every CAPA issue undergoes the same level of investigation.

Qualityze is been designed in adherence with the industry standards and also the best practices which is defined by the regulatory authorities that includes Standardization (ISO) – ISO 9001, ISO 13485 QMS software, Pharmaceuticals and Medical Devices Agency (PMDA), Therapeutic Goods Administration (TGA), China Food and Drug Administration (CFDA), etc. CAPA management software of the Qualityze is designed with an implementation task to help creating action plans which can eliminate or minimize the cause of the quality issue. Qualityze CAPA Management software helps you to conduct effectiveness reviews that ensure corrective actions or preventive actions implemented are working correctly. With this software you can also specify the verification plans to check the effectiveness of CAPAs.

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