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FAQ
> Glossary of Terms > M Series > Material
Containment
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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
MAb, Machine
Welding, Machine/Process
Lines, Macromolecules,
Macroparticles,
Macrophage, Macrorestriction
Map, Macroreticular
Resin, Maintainability,
Makeup Air, Manual
Welding, Manufacture,
Manufacturer, Manufacturing
Process, Manufacturing
Process(Biotechnology), Marker,
Material, Material
Containment, Maximum
Cr/Fe Ratio, Maximum
Depth of Enrichment, Maximum
Working Pressure, Mean
Kinetic Temperature(MKT), Mechanical
Code, Mechanical
Completion, Media
(plural of medium), Media
Preparation, Medical
Devices, Medicinal
Product, Medium
- Filter, Megabase-Mb,
Megohm, Meiosis,
Melanoma, Membrane,
Meristem, Messenger
RNA(mRNA), Metabolism,
Metabolite, Metadata,
Metaphase, Metastases,
Metastsis, Methods
Validation, Methyl
Cellulose, Mho, Microbe,
Microbiology, Microencapsulated,
Microinch, Micron
or Micrometer, Microorganism,
Microhmo, Milliequivalent,
Minienvironment,
Mitosis, Mixed
Air FLow Room, Mixed
Bed Ion Exchange, Moiety,
Moist Air, Molds,
Mole, Molecule,
Molecular Genetics,
Molecular Weight,
Monoclonal
Antibody(Mab or MoAb), Monomer,
Monosaccharides,
Mother Liquor, MSDS(Material
Safety Data Sheet), Multicellular,
Multiplexing, Multi-use
Equipment, Murine,
Mutagen, Mutagenesis,
Mutant, Mutation,
Mycelium, Mycobacterium,
Mycoplasma, Myeloma,
Mesophile
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- Material Containment
The method to incorporate suitable measures into design procedures
and operational practices for the containment of materials that
can harm personnel and the workplace environment, and minimize
potential for cross contamination and housekeeping concerns
in the fine chemical, bulk pharmaceutical and pharmaceutical
industries. Solids and/or liquids are normally most hazardous
in the form of powders and have been divided into the following
three categories:
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1. Biologically Hazardous additives are compounds
that when contacting a living cell, will alter, endanger,
or damage the cell in some shape or form. These should be
treated as requiring total containment.
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2. Chemically Hazardous additives are compounds
that when coming into contact with an oxidant, will cause
harm to its surroundings due to reaction and/or oxidation.
These products usually require containment and/or blanketing
with an inert gas.
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3. General Intermediates are compounds that
are neither biologically nor chemically hazardous additives
but they will cause a housekeeping problem. They usually require
dusting prevention.
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