Quality Control Solutions
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Container Closure Integrity Of Parenteral Products
7/9/2020
The United States Pharmacopeia USP 1207 guidance has been revised, encouraging the preference to deterministic, quantitative, and reliable non-destructive technologies to comply with quality standards.
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Pharmaceutical Powder/Fume Hood System
3/26/2019
Combination Powder and Fume Hood with HEPA filtration and house exhaust connection designed to process liquid and powder substances. Fume Hood designed to house stir plate and analytical balance. It features cup sink; air, water, and gas fittings; and alarm for monitoring and maintaining recommended face velocity of 75 LFPM. Fume and Powder Hoods separated by sliding door to eliminate cross-contamination during processing. Powder Hood uses front airfoils and rear plenums to maintain laminar airflow across the work surface, which is vented through a HEPA filtration system to house exhaust.
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Quality, Compliance, And Regulatory Services For Life Sciences
12/21/2020
The biotechnology, medical device, and pharmaceutical industries are highly regulated globally by a diverse group of agencies. Assuring GMP Quality and Regulatory Compliance throughout your supply chain is a challenge. Meeting this challenge requires a successful interaction between knowledge, systems, and people.
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FlexUP Technology Renewal Program: Keep Your Lab At The Forefront Of Science
4/11/2022
Choose the ideal mix of services with our FlexUP Technology Renewal Program for continuous operation in your laboratory and across your enterprise.
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Secure Your Pharma Analysis & QC
4/1/2022
Explore an extensive analytical chemistry and microbial testing compliant portfolio for pharmaceutical analysis and quality control (QC) from early-stage drug development to product release.
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Rapid Bioburden Testing System To Detect Microbial Contamination Earlier
4/7/2022
Traditional bioburden testing (or microbial limit testing) takes several days to grow visible colonies of microorganisms, so identifying these and initiating corrective action takes longer. The Milliflex® Quantum system quantitatively detects microbial contamination in filterable samples in as little as a third of the time it takes with traditional plate-based monitoring methods. The Milliflex® Quantum system is based on fluorescent staining of all viable microorganisms, making emerging microcolonies visible to the system when they’re still too small to be seen with the naked eye. After rapid detection, the colonies can be reincubated to grow into visible colonies and be identified by any method—an approach that cleverly combines rapid and compendial bioburden testing.
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Millipore P1000 x 500 x 500 Chromatography Column
5/17/2023
SKU: 3444-4
Manufacturer: Millipore
Location: Rhode Island
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Microbial Culture Media For Quality Control Of Non-Sterile Products
4/7/2022
Using the correct media is critical to ensure microbiological quality. Explore a portfolio of culture media and substances for sample preparation, microbial enumeration tests, and tests for specified microorganisms.
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Package Integrity Testing Systems For Tyvek and Porous Packaging
7/9/2020
Tyvek® gives the premium microbial barrier protection for sterilized medical instruments and pharmaceuticals. Apart from protecting the medical devices and pharmaceutical products from physical damages, medical and pharmaceutical packages also should provide an effective microbial barrier and help to maintain the sterility of the products. Bacteria and viruses with sizes varying from 0.002 to 100 microns are a constant threat to pharmaceuticals and medical devices which in turn can be hazardous to the patients.
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Container Closure Integrity Testing Using Gas Ingress
12/23/2019
The CCI Test Vessel provides a simple means of preparing samples for container closure integrity testing (CCIT) using the highly-sensitive and non-destructive laser-based headspace analysis technology. When combined with a LIGHTHOUSE FMS Headspace Gas Analyzer, the CCI Test Vessel offers a robust solution for container integrity tests on a wide range of container types and packaging conditions.