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Pharmaceutical & Cleanroom Glossary of Terms
A Series , B
Series , C Series , D
Series , E Series , F
Series , G Series , H
Series , I Series , K
Series , L Series , M
Series , N Series , O
Series , P Series , Q Series
, R Series , S
Series , T Series , U
Series , V Series , W
Series , X
Series , Y Series , Z
Series
First 1 - 45
Words, Next
46 - 90 Words, Pressure
Vessel, Pretreatment,
Primary Air, Primer,
Principle
of Nonrepudiation, Prions,
Probe, Procedures,
Process Aids, Process
Limits, Process
Suitability, Process
Support Systems, Process
Systems, Process
Validation, Process
Validation Protocol, Product
Campaign, Product
Contact Surface, Product
Mix, Product Water,
Production, Prokaryote,
Promoter, Prophylactic
Surgery, Prophylaxis,
Propylene Glycol,
Prospective Validation,
Prosthetic Groups,
Protease, Protein,
Protein Sequencer,
Proteolysis, Proteolytic
Enzyme(Protease), Proteomics,
Protocol, Protoplasm,
Protozoa, Psychrophile,
Psychrometer, Psychrometry,
Pseudonomas Diminuta, PTFE(Polytetrafluoroethylene)
Teflon, Public
Key Certificate(PKC), Pure
Culture, Pure Stream,
Purification, Purified
Water - USP, Purine,
Purity, PVC(Polyvinyl
Chloride), PVDF(Polyvinylidene
Fluoride), Pyrimidine,
Pyrogen
Learn About Deadly
Cancer Mesothelioma due to Asbestos Exposure, it can affect
any one in the world
Pseudonomas Diminuta
The bacterium used for validation of sterilizing filters. Recognized
as the challenge organism for 0.2µm filters, its size is 0.3 x 0.8µm
approximately. According to the HIMA (Health Industries Manufacturers
Association) standard, filters must be successfully challenged to
a titre of 107 per cm² to be validated as sterilizing grade 0.2µm
rated.
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