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Electronic Batch Record
Smarter Records, Faster Release
Aparev offers Electronic Batch Manufacturing Record (EBMR) solutions for pharma & biotech companies. Ensure compliance with 21 CFR Part 11 & EU GMP while improving efficiency and data integrity.
Our EBMR platform is designed to help manufacturers digitize batch processes, reduce paperwork, and stay audit-ready. By moving to a secure, paperless system, companies gain real-time visibility into production while maintaining strict regulatory compliance.
Key Benefits
- Compliance with global standards (FDA, EMA, WHO GMP)
- Faster batch release through digital QA review
- Secure electronic signatures & audit trails
- Integration with ERP, LIMS, and SCADA systems
- Reduced errors and increased efficiency
Electronic Batch Record
Smarter Records, Faster Release
Aparev offers Electronic Batch Manufacturing Record (EBMR) solutions for pharma & biotech companies. Ensure compliance with 21 CFR Part 11 & EU GMP while improving efficiency and data integrity.
Our EBMR platform is designed to help manufacturers digitize batch processes, reduce paperwork, and stay audit-ready. By moving to a secure, paperless system, companies gain real-time visibility into production while maintaining strict regulatory compliance.
Key Benefits
- Compliance with global standards (FDA, EMA, WHO GMP)
- Faster batch release through digital QA review
- Secure electronic signatures & audit trails
- Integration with ERP, LIMS, and SCADA systems
- Reduced errors and increased efficiency
Quality Management system
Quality Assured, Compliance Ready
Aparev offers Quality Management System (QMS) solutions to help pharma, biotech, and regulated industries maintain consistency, compliance, and continual improvement. Our QMS platform is designed to streamline quality processes, reduce risks, and ensure products meet the highest regulatory and customer standards.
By digitizing and centralizing quality management, organizations gain full visibility into quality events, audits, training, and corrective actions while ensuring compliance with ISO 9001, ICH Q10, and GMP guidelines.
Key Benefits
- Compliance with international standards (ISO, FDA, EMA, WHO GMP)
- Centralized document control with version management and access security
- Automated audits & CAPA workflows for faster resolution of issues
- Training management to ensure workforce competency
- Improved efficiency & traceability with electronic records and audit trails
Quality Management system
Quality Assured, Compliance Ready
Aparev offers Quality Management System (QMS) solutions to help pharma, biotech, and regulated industries maintain consistency, compliance, and continual improvement. Our QMS platform is designed to streamline quality processes, reduce risks, and ensure products meet the highest regulatory and customer standards.
By digitizing and centralizing quality management, organizations gain full visibility into quality events, audits, training, and corrective actions while ensuring compliance with ISO 9001, ICH Q10, and GMP guidelines.
Key Benefits
- Compliance with international standards (ISO, FDA, EMA, WHO GMP)
- Centralized document control with version management and access security
- Automated audits & CAPA workflows for faster resolution of issues
- Training management to ensure workforce competency
- Improved efficiency & traceability with electronic records and audit trails
Document Management system
Secure Documents, Easy Access
With Aparev’s Document Management System (DMS), your teams save hours spent searching, versioning, and securing critical documents. Designed for pharma, biotech, and regulated industries, our DMS ensures documents are always accessible, compliant, and audit-ready – reducing errors, saving manpower, and cutting operational costs.
Key Benefits
- Lower costs with paperless storage and retrieval
- Save time through version management and quick search
- Reduce manpower effort in handling compliance documents
- Enhance security with access control & audit trails
- Seamless integration with QMS, EBMR, and ERP systems
elogbook
Digital Logs, Total Traceability
Aparev’s eLogbook replaces paper-based logs with a secure, digital system that ensures traceability, saves staff hours, and improves compliance. Operators, supervisors, and QA teams can log, review, and approve activities in real-time, cutting delays and reducing the risk of human error.
Key Benefits
- Save time with real-time digital entries
- Cut manpower effort in maintaining manual logs
- Lower audit preparation costs with built-in traceability
- Ensure compliance with 21 CFR Part 11 & GMP
- Improve efficiency with instant logbook access anywhere
elogbook
Digital Logs, Total Traceability
Aparev’s eLogbook replaces paper-based logs with a secure, digital system that ensures traceability, saves staff hours, and improves compliance. Operators, supervisors, and QA teams can log, review, and approve activities in real-time, cutting delays and reducing the risk of human error.
Key Benefits
- Save time with real-time digital entries
- Cut manpower effort in maintaining manual logs
- Lower audit preparation costs with built-in traceability
- Ensure compliance with 21 CFR Part 11 & GMP
- Improve efficiency with instant logbook access anywhere
Data analytics
Clear Insights, Better Decisions
Aparev’s Data Analytics solutions give pharma and biotech manufacturers the power to turn data into decisions. By consolidating production, quality, and business data into actionable insights, companies save time, reduce costs, and make faster, evidence-driven decisions that improve compliance and efficiency.
Key Benefits
- Reduce costs with predictive analytics and process optimization
- Save manpower with automated dashboards & reports
- Accelerate decision-making with real-time insights
- Ensure compliance by monitoring deviations proactively
- Unlock growth through trend analysis and forecasting
Get Started
Where Pharma Meets Digital
Digitizing pharma with secure, compliant, and cost-efficient solutions that save time and reduce manpower.
