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BINDER™ APT-COM™ 4 Series
BINDER’s new Multi Management Software provides management, logging, programming, and documentation options, and much more. With features ranging from GLP-compliant logging to convenient program creation and management of up to 100 units, the APT-COM™ 4 can be used in all industries and makes complex work processes much easier.
Supplier: BINDER™ 90530042
Description
APT-COM™ 4 BASIC edition
- Administration of up to five connected units
- Log management (creating, deleting, archiving)
- Documentation of measured values
- Central overview of all units in both diagram and table form
- Graphical presentation of measured values
- Graphical/numerical program editor
- Manual export of measured values (CSV/PDF file)
- Multilingual user interface (German, English, French, Spanish, Italian)
- Optional program execution via APT-COM™
- Timer function
- Import of data from APT-COM™ 3
APT-COM™ 4 PROFESSIONAL edition
All the same functions as the BASIC edition and:
- Administration of up to 100 connected units at the same time
- Central overview of all units in a room plan
- Email-based alarm system
- Web server for displaying results
- User administration for multiple users and authorizations
- Automatic, time-managed export of measured values
- Reports for further processing/archiving
- Automatic/manual backup and recovery
APT-COM™ 4 GLP edition
All the same functions as the PROFESSIONAL edition and:
- Can be validated according to 21 CFR Part 11 including validation documents
- Documentation of measured values in a tamper-proof file in accordance with GLP/GMP guidelines on audit trails
- Electronic signatures
Specifications
Data Collection Software | |
Logging, Controlling, Monitoring | |
BINDER Chambers Series (BD, BF, CB-S, CB, CBF, ED, FD, FED, FP, M, KB, KB ECO, KT, KBF, KBF-S, KBF-S ECO, KBF P, KBF LQC, KBW, KBWF, UFV, VD, VDL) |
APT-COM | |
4 GLP-Edition Software | |
APT-COM™ 4 GLP-Edition - for working under GLP-compliant conditions. Measured values are documented in a tamper-proof way in line with the requirements of FDA Regulation 21 CFR 11. |
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