Our Quality Systems Documentation Services Include:

• Change Management System: Managing and documenting changes to processes, procedures, and systems to ensure consistency and compliance.
• Deviation Management System: Documenting and addressing deviations from standard procedures to maintain quality and compliance.
• Corrective and Preventive Action System: Implementing and documenting corrective actions to address issues and preventive actions to avoid future occurrences.
• Risk Assessment System: Identifying, assessing, and documenting risks to ensure they are managed effectively.
• Quality Manual, Water Manual, HVAC, and Clean Room Manual: Creating comprehensive manuals to document quality standards, water system requirements, HVAC systems, and clean room protocols.
• Documentation Control System: Managing and controlling documents to ensure they are accurate, up-to-date, and accessible.
• Quality Policies and Objectives: Developing and documenting quality policies and objectives to guide organizational practices and goals.
• Quality Culture and its Indicators: Documenting and promoting a quality culture within the organization and identifying key indicators of quality performance.
• Complaint Handling System: Establishing a system for documenting and managing customer complaints to improve service and product quality.
• Audit Handling System: Preparing and documenting procedures for handling audits to ensure compliance and address findings effectively.
• E-logbook System: Implementing electronic logbooks for accurate and efficient documentation of activities and data.
• ISO System: Developing and documenting processes to meet ISO standards and achieve certification.
• QMS Principles: Documenting the principles of Quality Management Systems (QMS) to ensure effective quality management.
• Process Performance and Product Quality Monitoring System: Monitoring and documenting process performance and product quality to maintain high standards.
• BMR – Batch Manufacturing Record System: Creating detailed records of batch manufacturing processes to ensure consistency and compliance.
• BPR – Batch Packaging Record System: Documenting batch packaging processes to ensure product integrity and compliance.

Why Choose Pharma-Zon for Quality Systems Documentation?

• Expertise: Extensive experience in documenting quality systems across various industries.
• Comprehensive Solutions: Wide range of documentation services to cover all aspects of quality management.
• Compliance Focused: Ensuring all documentation meets industry standards and regulatory requirements.
• Tailored Approach: Customizing documentation solutions to fit your organization’s specific needs.