We have over 30 years of experience in testing of various products or substances in different industries like Pharmaceuticals, chemical, beauty care products, wellness, cosmetics, nutraceuticals, over the counter and consumer products. And we apply our total Quality Assurance expertise to give best results and within proper time.

We at Chromak Research, provide advanced research and testing expertise, and operate under ISO 17025, Good Laboratory Practice (GLP), Good Manufacturing Practice (cGMP) and other recognized industry standards. we ensure that our every product and service comply with global standards and local regulations. We perform testing protocols according to standard methodologies (ISO, EN, BP, ASTM, FCC, etc.) and are experts in developing tailored analytical methods and performing method validation for specific testing applications.

Every Industry needs testing and analysis of their products as well as raw materials for regulatory compliance and to understand the quality and composition of chemical substances. Our laboratories are fully equipped with state-of-the-art analytical instrumentation including ICP-MS, LC-MS, GC-MS, HPLC, GC with Headspace, TLC, UV, IR, Polarimeter, Refractometer, muffle furnace, vacuum ovens, stability chambers and Amino Acid Analyzer. Company has also an extensive network of testing partners to meet most analysis requirements.

Chromak services to various industries in complete analysis includes

  • USP 1663 &1664 Extractables & Leachables studies
  • Identification of products to check its purity, safety and efficacy
  • Unknown Contamination testing
  • Impurity Identification in complex formulation
  • Microbial testing
  • USP 661.1, 661.2 & 671 testing for CCS
  • USP 232 & 233 Elemental Impurities by ICPMS
  • USP/NF Monograph testing for Pharmaceuticals Active & Inactive Raw materials.
  • 21 CFR 176 (Indirect Food Additives)
  • De-formulation & Reverse engineering
  • Method development, Validation & Method transfer
  • Amino acid analysis (Peak X detection in 5-Hydroxy-L-Tryptophen (5-HTP) as per FDA methodology)
  • Enzyme Activity Assay
  • Cleaning Validation
  • Stability Testing