Pharmaceutical QC
Constant vigilance is needed throughout the production of pharmaceutical products, from the initial use of qualified raw materials to the release of safe and effective finished product. Pall is involved in every stage of the development and production of the product, including monitoring and ensuring that final product meets required purity and safety targets. In order to ensure that requirements for product sterility or low bioburden and absence from other contaminants are met, both product quality and the manufacturing environment in which it is made is monitored constantly.Pall's Pharmaceutical QC Product CapabilitiesPall is increasingly involved in quality monitoring. Product groups include:
Pall® quality control and monitoring systems are characterized by their ease-of-use, pre-assembled and ready to use consumables (detailed within each product’s technical description and specifications), full documentation and validation packages, operator training support and the availability of local technical support and service - wherever you are in the world. |
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Pall's Pharmaceutical QC Services
In addition to a growing product portfolio, Pall’s Technical Centers are available to our customers for a variety of contract services.- Contamination Analysis
- Process Development and Optimization
- Bacterial Removal Validation
- Virus Removal Validation
- Contaminant Removal Validation
- Troubleshooting and Consultation
- Pre-Inspection Reviews
Pall Allegro Sampling Containers, Ports and Systems
The Allegro™ biocontainer range and associated systems include small bags (50 mL capacity), manifolds, ports and connectors designed for taking samples from a variety of points during the pharmaceutical production process.Allegro Single-use Systems can include additional biocontainers and connections for integrated sampling and integrity testing as part of the system, ensuring product safety and security.
Information on the full range of Allegro single-use systems is available here.



