As a pharmaceutical company, you help to enrich and extend life across all disease areas.
Implementing a decent electronic Quality Management System helps you to digitize and organize numerous linked processes, according to cGMP requirements: Corrective and Preventive Action (CAPA), Non-Conformance Management, Internal and External Audit Management, Risk Management, Complaint Management, Document Control, Incident Management, Calibration Management, Management of Product Releases, Management of Recalls, Management of Returns, Management of Samples, Training Management, Management of Change (MoC).
It has been proved that both the software and the customized applications are able to be qualified for use in a pharmaceuticals environment.
Internal monitoring and auditing of business processes help to detect and prevent potential violations of best practices.
Prompt response and corrective action for detected problems are keynotes in your daily commitment to quality, safety, and ethics.
With BizzMine you have validated QMS software according to international standards.
Measure up to stringent legislation and government requirements and meet all quality requirements and regulations according to cGMP and FDA in one flexible platform.
Streamline operations, be more resilient and build a sustainable business.
Download the whitepaper
BizzMine helps you to better organize and follow up your internal and external audits.
BizzMine helps you to continually improve the effectiveness of your QMS.
BizzMine helps you to better manage and control all data on training and competencies.
Track, investigate, and correct your customer and supplier complaints.
BizzMine is the perfect application to plan, organize and analyze all calibration processes.
Centralized management of SOPs, manuals, work instructions and other documents.