Multiparameter Measurement System:
Pharma Measurement Systems
-
-
-
- +4
- Fully automatic measurement with market-leading precision
- Sample recovery unit available to minimize product loss
- Full compliance with Pharmacopeia regulations
- Guaranteed data integrity and traceability
- DMA 5000 M, Xsample 530, Abbemat Performance 500, Lovis 2000 ME
Complex measuring tasks meet modular multiparameter measurement systems: The Pharma Measurement System combines the measurement of density, refractive index, and viscosity with a versatile sample changer. Choose from the various combinations of the superior density meters and refractive index measurement instruments based on your specific application requirements. Comprehensive software features for the requirements of the pharmaceutical industry help to avoid measurement errors, to track every action with the instrument, and to keep the data safe. This easy-to-handle, automized quality control measurement system helps you save costs.
Key features
Efficiently streamline lab operations
Density, refractive index, and viscosity from one sample and one filling – this is the power of the Pharma Measurement System. The highly flexible measuring setup can be adapted to measure only the parameters needed. Due to its full modularity, explore combinations with the Polarimeter MCP, as well as additional modules such as the pH measuring module pH ME or the turbidity meter HazeQC ME. This efficient combination is capable of saving up to 80 % of your valuable working time in the lab compared to manual methods.
Full compliance with Pharmacopeia regulations
The Pharma Measurement System combines a state-of-the-art density meter, a refractometer, a rolling-ball viscometer and a sample changer in one system. The measuring technology of these modules conforms to all major pharmacopeia regulations. This means full compliance and traceability, allowing you to focus on your measurement tasks while all relevant actions taken are supervised by the incorporated user management and documented in an audit trail.
Full traceability at every step
The “what, when, why, and who” of every step of your instruments need to be documented according to GMP regulations and for later audit purposes. In the Pharma Measurement System’s software, measurements, checks, adjustments, changes of instrument settings, users, and methods are tracked in a comprehensive audit trail. Fully customizable user and role management with individually configurable permissions and password rules according to your requirements allows for a clear attribution of any action to a specific user. This way you maintain full overview and benefit from simple review possibilities.
Keep your data safe – guaranteed integrity and traceability
Embedded software features in the modular system from Anton Paar – like the advanced data integrity mode – help you avoid loss of data.
The software package AP Connect Pharma connects your instruments, collects data and audit trails, and manages them accordingly. It allows for user-centered data review and approval processes, which can even be performed remotely. The program offers simple search and filter options for the entries and automatic export to connected LIMS systems. Needless to say, the electronic signature is fully 21 CFR part 11 compliant. Since you don’t have to worry about data availability and accessibility, you can dedicate your time to data quality and making key decisions.
Minimal time to get ready for operation
The Pharma Measurement System offers straightforward and fast setup for operation. System installation, user and applicative training by well-trained Anton Paar staff together with the available pharma qualification packages and qualification services by specialists, help you simplify your own qualification process and to save weeks and months of time.
Degree of automation – adjust your level of individuality
High sample throughput and different measurement requirements can be challenging. The Pharma Measurement System is equipped with a versatile sample changer. Not only does it allow reproducible and repeatable filling of even difficult samples (e.g. higher viscosity, hazardous components) into the measuring modules, but it can also properly and traceably clean and check them afterwards. This frees up valuable resources for other tasks in your laboratory.
Standards
US Pharmacopoeia (USP)
European Pharmacopoeia (Ph. Eur.)
Japanese Pharmacopoeia (JP)
Chinese Pharmacopoeia (ChP)
Standards
US Pharmacopoeia (USP)
European Pharmacopoeia (Ph. Eur.)
Chinese Pharmacopoeia (ChP)
Japanese Pharmacopoeia (JP)
Standards
US Pharmacopoeia (USP)
European Pharmacopoeia (Ph. Eur.)
Japanese Pharmacopoeia (JP)
Chinese Pharmacopoeia (ChP)
Anton Paar Certified Service
- More than 350 manufacturer-certified technical experts worldwide
- Qualified support in your local language
- Protection for your investment throughout its lifecycle
- 3-year warranty
Documents
-
Assessment of quality control measurements for disinfectants and hand sanitizers Application Reports
-
E-Book - The Field Guide to Data Integrity in Regulated Industries Application Reports
-
Quality control and stability monitoring of vitamin C-containing cosmetic serums Application Reports
-
Quality control of substances from pharmacopeial monographs Application Reports
