Quality Segment
product line
EMPROVE® EXPERT
assay
50%
form
liquid
density
1.24 g/cm3 at 20 °C
application(s)
cleaning in place
pharma/biopharma processes
storage temp.
15-25°C
General description
Every bio-manufacturing process involves cleaning to protect equipment and prevent cross-contamination. All our GMP (IPEC/EXCiPACT) solutions for CIP and buffer preparation are manufactured under Excipient GMP conditions and feature low bioburden levels, backed by our Emprove® Program for exceptional quality and documentation support.
As a result, you can integrate our solutions directly into your biopharmaceutical production process. In addition to our comprehensive portfolio, we also offer custom manufacturing services to meet your exact needs.
As a result, you can integrate our solutions directly into your biopharmaceutical production process. In addition to our comprehensive portfolio, we also offer custom manufacturing services to meet your exact needs.
Application
Citric acid 50% is used in the CIP process of biopharma manufacturing to effectively lower pH, chelate metal ions, and dissolve mineral deposits, ensuring thorough cleaning of equipment.
Features and Benefits
- Comprehensive, up-to-date documentation you need to navigate regulatory challenges, manage risks, and improve processes.
- Suitable for higher-risk applications where the lowest microbiological and endotoxin levels are of utmost importance.
- Emprove® products are designed to facilitate compliance with global regulations (e.g., ICH Q7, EU GMP, USP, EP).
- Detailed supply chain and manufacturing information helps ensure traceability and continuity, which is critical for GMP manufacturing.
Legal Information
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
Hazard Classifications
Eye Irrit. 2 - STOT SE 3
target_organs
Respiratory system
保管分類
12 - Non Combustible Liquids
hcodes
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