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Supplier: Cole-Parmer
Description: Climatic Simulation Chamber, 25.4 cu ft. Chambers meet International Conference on Harmonization (ICH) standards for new drug stability testing DCTreg cooling system prevents chamber icing and condensation Patented preheating technology eliminates hot and cold spots Symmetrical airflow
- Test Chamber Style: Benchtop / Instrument
- Test Parameters: Temperature, Humidity
- Features: Shelves
- Type: Environmental Stability
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Supplier: Jeio Tech, Inc.
Description: Constructional Features High quality #304 stainless steel exterior and interior. Casters for easy mobility when installing or moving environmental test chamber. Convenient maintenance - Available to check total operating time. Unique door lock & trim. Vice lock type door and foam
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Supplier: Caron Products and Services, Inc.
Description: technical innovations. These units have a wide temperature and humidity range and are designed in accordance with ICH Q1A guidelines, making them perfect for pharmaceutical stability drug testing. Caron's Environmental Test Chambers are also ideal for numerous other applications
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Supplier: Fritsch GmbH - Milling and Sizing
Description: with extremely high air throughput Wear-free rotor made of stainless steel capable of accepting extreme loads Wear-free labyrinth seal between grinding chamber and drive motor High speed stability even under full load Conversion kit for iron-free grinding Equipment As a standard you receive
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Supplier: Shimadzu Scientific Instruments, Inc.
Description: Triple Quadrupole Mass Spectrometry is the method of choice for accurate quantification and confirmation of trace level analytes in complex matrices. From the detection of drugs and metabolites in biological specimens to environmental contaminants and pesticides in food, analysts the world over
- Mass Analyzer Design: Quadrupole
- Ionization Method: Electrospray Ionization (ESI)
- Interfaces with a Liquid Chromatograph (LC): Yes
- Local Interface: Digital Front Panel
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Supplier: Micromeritics
Description: accommodated. Changes in sample mass of 0.1μg and unrivalled long-term stability are hallmarks of the Intrinsic and which are required for the accurate measurement of water sorption phenomena. These measurements may take from a few minutes to a few hours to complete depending upon the sample size
- Property Analyzed: Adsorption / Desorption (Chemisorption/ Physisorption)
- Test Media / Material: Building & Construction Materials, Concrete / Cement, Food / Drugs, Porous Materials (Filters, Foam, etc.), Rock / Aggregate, Wood / Wood Product
- Display & Special Features: Computer Interface / Networkable, Laboratory / Batch
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Featured Products for Drug Stability Chamber Top
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Parameter Generation & Control, Inc.
30 Cubic Foot Photostability Chamber
. The ballasts for the visible and UV lamps are interchangeable. The lamps can be replaced to convert from one type of light source to another. (If the automatic light control feature is purchased the light sources are not interchangeable). Each shelf will adhere to photo stability requirements as defined in the International Conference on Harmonization (ICH) Guideline Q1B entitled Guidance for Industry Q1B Photo Stability Testing on New Drug Substances and Products. Maximum usable height from light... (read more)
Browse Stability Chambers and Rooms Datasheets for Parameter Generation & Control, Inc. -
Parameter Generation & Control, Inc.
Pharmaceutical Rooms / Walk-Ins
ON-SITE STABILITY STORAGE ROOMS FOR PHARMACEUTICAL COMPANIES. Each Parameter pharmaceutical room is custom built to meet ICH and FDA guidelines for storage conditions for pharmaceutical products. Our rooms are used by many drug companies for active substances stability studies, stress testing, photostability testing and degradation examinations. We understand how a loss of a long-term stability study can impact operations. As your single-source provider of planning, designing, building, testing... (read more)
Browse Environmental Test Chambers and Rooms Datasheets for Parameter Generation & Control, Inc. -
Quantachrome Instruments
Aquadyne DVS
sample chamber ensures rapid changes in sample atmosphere conditions when the relative humidity is altered during an analysis. Sample(s) can be pre-dried in situ at up to 80degC in a flow of dry gas. The software supports multiple users with password-controlled access. Stability of pharmaceutical excipients and drug actives. Drying and storage of grains. Texture and shelf life of food products. PEM fuel cell components. Mortar, grout and other cementitious materials. Paper and coatings... (read more)
Browse Property Testing Equipment Datasheets for Quantachrome Instruments -
Rotronic Instrument Corp.
ROTRONIC HP23-AW-A Water Activity Measurement
the corresponding moisture content at a given constant temperature. Each product has its own sorption isotherm. Water migration: The aw of a product will always try to reach equilibrium with the surrounding atmosphere. Water will migrate from regions with a high aw to the regions of low aw. Water will migrate until equilibrium is reached!. The effect of water in foodstuffs: Water is also recognised in the food industry as being critical for the stability of most products. aw exerts a decisive influence... (read more)
Browse Humidity Measurement Instruments Datasheets for Rotronic Instrument Corp.
Conduct Research Top
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Choosing the Proper Equipment for Pharmaceutical Stabililty Room Humidity and Temperature Mapping
of shelf life. Humidity,. temperature, light and other conditions can cause drugs to degrade or lose their efficacy. before reaching the consumer. Stability testing is usually performed in some type of. environmental chamber which allows for changing conditions of humidity and. temperature
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Room Mapping
Temperature and humidity levels that are out of Specifica-tions can cause damage on production material and even on final the product. You can imagine that this is very impor-tant for phar-maceutical companies. The public regulatory or-ganizations (see table on the right ) re-quire food and drug
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How to Respond to (& Avoid) FDA 483s (.pdf)
. variety of GxP settings; they range. manageable) with some links to. from failure to properly validate. further resources. Finally, we'll look. containers for Human Cell & Tissue. Sample Deviation #1. To a Contract Pharma manufacturer: "Requirements for stability testing of drug products
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How to Avoid (and Respond to) FDA 483s
) with some links to. from failure to properly validate. further resources. Finally, we'll look. containers for Human Cell & Tissue. Sample Deviation #1. To a Contract Pharma manufacturer: "Requirements for stability testing of drug products are not. being met. For example, you do not have, as part
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Water activity in the food industry
and Microbial stability, L.R. Beuchat. Application note: N°F004. July 2011. What solutions can Rotronic offer?. Water activity or equilibrium. Leak proof measurement. 0.8aw at 25°C with a 1°C. relative humidity is usually. chamber: closed system. temperature difference can. defined as the percent rela
Engineering Web Search: Drug Stability Chamber Top
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Guidance for Industry: Nonsterile Semisolid Dosage Forms
U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) May 1997 SUPAC-SS CMC 7
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MDI and DPI Drug Products
U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) October 1998 CMC
- Stability Chambers and Rooms Information on GlobalSpec
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Drug Makers Fight Back! On GlobalSpec
Home > Technical Library > Drug Makers Fight Back! Drug Makers Fight Back! Print Share via Email
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Extrusion - Wikipedia, the free encyclopedia
3.5 Drug carriers 3.6 Biomass briquettes
- Nanoparticle - Wikipedia, the free encyclopedia
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Blue M CEO Series Steady State Food Drug Stability Test...
Blue M CEO Series Steady State Food Drug Stability Test Chamber Blue M CEO Series Steady State Food and Drug Stability Chamber Photo Gallery
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Stability Chamber
Stability Test Chamber LABTOP Stability Test
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Characterization of the hydration state of pharmaceuticals by...
of hydration of a drug can effect its solubility, dissolution rate, bioavailability, chemical stability, and the physical stability of subsequent
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Stability Testing, Accelerated Aging Testing - CSZ...
Test Chamber Capabilities Test Specifications
