Raw Materials and Excipient Testing
Product Description
Chromak Research Inc.
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Country/Region:United States
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On CPHI since:2026
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Certificates:2
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Employees:1 - 24
Company types
Primary activities
Categories
Specifications
Chromak Research Inc.
-
Country/Region:United States
-
On CPHI since:2026
-
Certificates:2
-
Employees:1 - 24
Company types
Primary activities
More Products from Chromak Research Inc. (39)
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Product Genotoxic Impurity analysis
Genotoxic impurity analysis is undeniably an important factor for testing within the pharmaceutical industry and in any chemical-derived products. Genotoxic impurities (GIs) are, even in trace quantities, DNA-reactive elements that have the propensity to damage one’s genetic material. They possess the capa... -
Product Impurity Identification
Considering life sciences and pharmaceutical companies, product cleanliness is not merely a ‘compliance burden’; it significantly threatens patient health and product efficacy. The evaluation of impurities is one of the prime activities of quality assurance (QA) and quality control (QC) functions in drug d... -
Product Infrared (IR) Spectroscopy Testing
Infrared (IR) Spectroscopy technologies performed at Chromak Research facilities are one of the most common IR based analytical techniques to evaluate and identify chemical compounds. It is IR Spectroscopy and measures the interaction of infrared radiation with matter through absorption, emission, or refle... -
Product Method Development & Validation
Within the context of drug product and substance testing, method development and validation constitute the backbone of the analytical work as well as the legal framework. Chromak Research is a prominent contract testing laboratory. We design and validate analytical methods for ensuring the quality, identit... -
Product Nitrosamine Impurities Testing
Nitrosamine impurities pose a great risk since they are most likely carcinogenic to humans. Nitrosamines are compounds formed from the reaction of a nitroso group with an amine. Nitrosamines are produced during the interaction of secondary amines, amides, carbamates, urea derivatives, nitrites, or other ni... -
Product Potentiometric & Karl Fischer Titration
Chromak Research, we offer low-cost Potentiometric Titration and Karl Fischer Titration services with extreme accuracy. These approaches are commonly used for determining the assay, purity, and moisture content of samples from pharmaceutical, chemical, food, and other industries. -
Product Research & Development
Research and Development (R&D) is at the heart of innovation, improvement, and success in products across all sectors. At Chromak Research, we understand the sheer need for quality, compliant, and successful R&D services specifically for pharmaceutical, nutraceutical, cosmetic, and industrial produ... -
Product Residual Solvents Analysis
Residual solvents are organic volatile chemicals used or formed during the course of drug substance, excipient, and pharmaceutical product manufacture. They are never completely removed during manufacturing and, if not controlled, their existence can compromise product safety, quality, and regulatory stand... -
Product Stability Storage and Testing Program
Stability Storage and Testing Program at Chromak Research to meet the high standards of the pharmaceutical, chemical, and manufacturing industries. With well over 30 years of experience in the industry as a premier contract testing laboratory, Chromak Research conducts stability testing to establish the sh... -
Product Toc analyzer
Chromak Research offers reliable and accurate TOC analyzer testing to diverse industries like pharmaceutical, biotechnology, cosmetics, and environmental. Our laboratory uses advanced Total Organic Carbon (TOC) analyzers to detect and quantify organic impurities in water samples for regulatory compliance a... -
Product UV visible spectroscopy
UV-Visible Spectroscopy, also known as Ultraviolet-Visible Spectroscopy (UV-Vis), is a general and widely utilized analytical technique in scientific research and industrial laboratories. It measures the absorbance or transmission of a substance at specific UV and visible wavelengths and produces valuable ... -
Product Antimicrobial Effectiveness Testing (AET) – USP <51>
Antimicrobial Effectiveness Testing (AET) or Preservative Effectiveness Testing is an essential quality control procedure for sterile and nonsterile aqueous drug products. It is performed to determine the effectiveness of the antimicrobial preservatives incorporated within the formula to retard the growth ...











