Environmental Monitoring Compliant with Pharmaceutical Regulations
OpreX Environmental Monitoring System collects, measures, and stores data such as temperature and humidity as well as other management data to monitor the environment in pharmaceutical manufacturing area, quality control area, and storage area.
Major features
Data Integrity
- Meets ALCOA+ requirements
Data Collection and Long-term Storage
- Long-term storage of collected data in recorders that are FDA 21 CFR Part 11 compliant
Real-Time Data Monitoring
- Monitor measured data and alarms using the monitoring software
Centralized Management for Login User
Centralized management of user names and passwords using servers on the network is possible through Active Directory.
- Centralized management of user name/password in Data Server and recorders
- User login access control
Packages
Data Management Package
Centralized management of the recorded data file
Access Control
Users are assigned to groups and are given access privileges based on the group they belong to.
Only authorized users can login to the system and search and browse through data.
Audit Trails
All file operations by an authorized user are recorded in the audit trail.
- File operations (Archive, Delete)
- Backup and Restore
Configuration Tool
Adminstrator configures the Data Management Package using this tool.
- Register new recorders
- Register new users
- License management
GA10 Real-time Monitoring Software
Monitor measured data in real time
- Measured value display (Trend display / Digital display)
- Alarm notification on the screen
- Monitor data for each measurement group
Universal Viewer
Dedicated viewer software for browsing recorded data
- Display recorded data
- Supports latest OS and offers best viewing quality
- Supports 7 languages
Paperless Recorder
SMARTDAC+ Series
Measure and record a variety of data
- Add I/O modules as needed
- Wide variety of powerful display functions
- A full range of network functions
Advanced Security Function
Electronic recording of data is compliant with pharmaceutical regulations
- Logical security
- Audit trail function
- Secure data storage in binary format (fraud proof)
- Dedicated viewer software
Publikationen
Chugai uses the Pharmaceutical Model DX200P Data Acquisition Station for storage quality control of investigational drugs and ingredients.
Videos
YOKOGAWA aspires to establish Smart GMP manufacturing facilities that provide consistent quality and supply while eliminating industrial waste, enhancing productivity and always using high-quality component parts and materials.
By equipping SMARTDAC+ with the advanced security features option "/AS", it meets the strict requirements of the U.S. FDA 21 CFR Part 11 and supports DI in compliance with PIC/S and ALCOA+ by WHO, MHRA and FDA.
By adopting the environmental monitoring system, we were able to create an environment in the cell storage facility that allows for quality control, maintaining a high level of safety.
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