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Difference between GMP and cGMP

  To cut to the point, the difference between GMP and cGMP is that GMP requires manufacturers to ensure that their products are safe and effective. cGMP requires manufactures to employ technologies and systems that are up to date and comply with GMP regulations. Why GMP is known as cGMP? GMP is also sometimes referred to as "cGMP".  The "c" stands for "current," reminding manufacturers that they must employ technologies and systems which are up-to-date in order to comply with the regulation . Why C is small in cGMP? 1 Answer. “c” should be written in small letters as  it is dynamic and it changes . This is from another site: GMP is also sometimes referred to as “cGMP”. The “c” stands for “current,” reminding manufacturers that they must employ technologies and systems which are up-to-date in order to comply with the regulation.
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solvents boiling points

 solvents boiling points : Solvent Boiling Point (°C) Solvent Boiling Point (°C) Acetic Acid 118.0 Ethyl Acetate 77.1 Acetic Acid Anhydride 139.0 Ethyl Ether 34.6 Acetone 56.3 Ethylene Dichloride 83.5 Acetonitrile 81.6 Ethylene Glycol 197.5 Benzene 80.1 Heptane 98.4 iso-Butanol 107.7 n-Hexane 68.7 n-Butanol 117.7 Hydrochloric Acid 84.8 tert-Butanol 82.5 Methanol 64.7 Carbon Tetrachloride 76.5 Methylene Chloride 39.8 Chlorobenzene 131.7 MTBE 55.2 Chloroform 61.2 Pentane 36.1 Cyclohexane 80.7 Petroleum Ether 35.0-60.0 Cyclopentane 49.3 iso-Propanol 82.3 Dichloromethane 39.8 n-Propanol 97.2 Diethyl Ether 34.6 Pyridine 115.3 Dimethyl Acetamide 166.1 Tetrahydrofuran 66.0 Dimethyl Formamide 153.0 Toluene 110.6 Dimethyl Sulfoxide 189.0 Trifluoroacetic Acid 71.8 Dioxane 101.0 Water 100.0 Ethanol 78.3 Xylene 140.0
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What is 21 CFR Pharma

  The Code of Federal Regulations (CFR) is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the Federal Government.. Title 21 of the CFR is  reserved for rules of the Food and Drug Administration . What is the purpose of 21 CFR Part 11 21 CFR Part 11 is the FDA's regulations for electronic documentation and electronic signatures. It  outlines the administration of electronic records in a medical device company's quality management system .
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DATA INTEGRITY

  The ALCOA Principles ALCOA is an acronym for the original five principles of data integrity. Those principles are: Attributable Legible Contemporaneous Original Accurate However, the original ALCOA principles have since been updated to ALCOA+. The original principles remain with four additions: Complete Consistent Enduring Available
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Centrifuge operation:

  Centrifugation  uses gravity and centrifugal force to separate particles heavier than the liquid medium . Centrifuges spin the material at high rotation speeds and separate the particulate from the liquid.
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Agitated nutsche filter and drying (ANFD) :

  Agitated nutsche filter and drying (ANFD) : Agitated Nutsche Filter with drying is a closed vessel special designed to  separate solid and liquid by filtration under pressure or vacuum . The ANFD closed system ensures odorless contamination free & non-polluting working condition maintaining products purity as well hygiene.
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sop

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