Usp Purified Water Vs Wfi

Control of the chemical purity of these waters is important and is the main purpose of the monographs in this compendium.

Usp purified water vs wfi.

As previously discussed because of the volume of water actually tested 1ml for endotoxins vs. From usp 1231 water for pharmaceutical purposes. Specification as per usp. Distilled water water for injection sterile distilled water sterile wfi.

Conductivity 1 3 µ s cm at 25 0 c 1 3 µ s cm at 25 0 c total organic carbon toc 500 ppm 500 ppm microbial recommended action limit 100cfu ml 10cfu 100ml endotoxin. Wfi has stricter bacteria controls than purified water and hence the usp mandates these waters should have less than 500 ppb of total organic carbon fewer than 0 25 eu ml endotoxins and a conductivity of less than 1 3 us cm 25 c. Purified water and sterile purified water may be obtained by any suitable process. The type of water for pharmaceutical use is determined by usp testing.

The procedure described below is designed for measuring the conductivity of purified water and water for injection. Unlike other official articles the bulk water monographs purified water and water for injection also limit how the article can be produced because of the belief that the nature and robustness of the purification process is directly related to the resulting purity. Sterile water for injection see the usp monograph is water for. 100ml for wfi the microbiological test offers a good index of the level of contamination in a system.

Stage 1 of the procedure below may alternatively be performed with the appropriate modifications to step 1 using on line instrumentation that has been appropriately calibrated whose cell constants have been accurately determined and whose temperature compensation function has. Regulatory agencies have required that packaged pw and wfi be tested by the producer using toc and conductivity prior to packaging. Pharmaceutical technology is the independent source for information insight and analysis on bio pharmaceutical formulation development and manufacturing. The usp purified water and the usp wfi on the other hand are components or ingredient materials as they are termed by the usp intended to be used in the production of drug products.

Water for injection is water purified by distillation or reverse osmosis. Action levels in usp 1231 100cfu ml for purified water and 10cfu 100ml for water for injection are generally considered to represent a level above which the water is unfit for use.