Discover Alfa Laval UltraPure Pumps
Alfa Laval UltraPure pumps are specifically designed for the toughest, most demanding pharmaceutical applications. From high-value, high-risk productions where every second counts to reliability and repeatability process-driven productions, whatever your challenge, there’s an Alfa Laval UltraPure solution to meet your needs.
Discover Alfa Laval UltraPure Pumps:
Safety
Alfa Laval UltraPure pumps feature a high level of attention to hygiene and repeatability to reduce the risk of contamination.
Reliability
Time-tested and proven designs guarantee the repeatability and quality of your product.
Efficiency
Alfa Laval UltraPure pumps are cost-effective pumps that deliver maximum energy efficiency, a reduced C02 footprint, higher yields and increased uptime.
Global coverage with local presence
Our wide range of Alfa Laval UltraPure pumps can meet your any of your process challenges. No matter where you are, Alfa Laval’s service and support experts are always close by and ready to help, everything you need close at hand.
Discover Alfa Laval UltraPure Pumps
Documentation for biotech and pharmaceutical needs
The standard Alfa Laval Q-doc documentation package for Alfa Laval UltraPure equipment ensures full traceability of all product contact parts such as, steel, gaskets, etc. This secures a perfect match every time and prevents potential oversights that could necessitate a revalidation.
Alfa Laval Q-doc comprises conformity declaration, material certificates, relevant test certificates and information about Alfa Laval spare parts kits for standard components. Our Q-doc documentation package supports a smooth qualification and validation process, and safeguards long-term peace of mind.
Need to find documentaton for your Alfa Laval UltraPure pump?
All Alfa Laval UltraPure pumps are supplied with Alfa Laval Q-doc, our documentation package providing full traceability of all product contact parts such as steel, gaskets, etc. Alfa Laval Q-doc secures a perfect match every time and prevents potential oversights that could necessitate revalidation.