USP 1231 Standard Test Method for Pharmaceutical Water

EUROLAB laboratory provides testing and compliance service within the scope of USP 1231 standard. Water is widely used as a raw material, inactive ingredient, medical tool and solvent in the processing, formulation and manufacture of pharmaceutical products (dosage forms), active pharmaceutical ingredients (APIs), API intermediates, supplemental articles and analytical reagents.

This is an informative section on pharmaceutical water issues and includes some of the chemical and microbiological concerns specific to water, its preparation and use.

This section provides information on water quality attributes (which may or may not be included in a water monograph) and treatment techniques that can be used to improve water quality.

It also discusses water system verification and gives a description of the minimum water quality standards to consider when choosing a water source, including sampling and system checks.

It is equally important to operate and maintain water systems in a controlled state to ensure operational stability and therefore the ability to provide water that meets established water quality standards.

EUROLAB assists manufacturers with USP 1231 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.