Infrared (IR) Spectroscopy 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 Elemental Impurities
Chromak Research are experts in the critical evaluation and testing of elemental impurities to ensure the safety and efficacy of pharmaceuticals. Elemental impurities are trace amounts of metals like lead, arsenic, and cadmium, which may be toxicologically relevant. Such impurities from diverse sources cou... -
Product Enzyme Activity Assay
Enzyme activity assays are essential in the pharmaceutical field, especially in drug development, research, and product compliance. By definition, an enzyme is a catalyst, most often a protein, that facilitates chemical reactions within living organisms. A living cell is loaded with biological works, and s... -
Product Extractables & Leachable studies
Chromak Research posits that the health of patients is as important as the rigorous testing and scrutiny that goes behind pharmaceutical and medical device products. Extractables and leachables testing are an essential part of the procedure as they deal with potential risks that need to be solved in regard... -
Product Gas Chromatography
Gas Chromatography Testing, commonly known as GC testing, is an analytical technique used to separate, identify, and quantify chemical constituents of interest from various samples. It can analyze trace complex chemical mixtures and smaller amounts of various compounds that could be present in a sample. GC... -
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 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 Raw Materials and Excipient Testing
Biopharmaceutical and pharmaceutical industries, product quality commences well before the last step of assembling the dosage form. It starts with checking the safety and efficacy of the raw materials and excipients. At Chromak Research Inc. (CRI), we provide fully pharmacopeial-compliant excipient and raw... -
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...