Chemical Evaluation

In accordance with the rules of the US EPA, US FDA, the European CE and MDR, and non-EEC nations, the chemical and quality control laboratory at CMDC Labs conducts tests on raw materials, cosmetic items, medical devices, materials in contact with food, toys, and other consumer products.

In accordance with all relevant laws, CMDC Labs creates customized research protocols and conducts transdisciplinary tests in accordance with the notified body guidelines for pharmaceuticals, cosmetics, and medical devices.

Thanks to a wide range of certified tests, sophisticated instruments make it possible to meet customer needs.

Chemical testing provided by CMDC Labs:

  • Instrumental analysis includes the use of HPLC and UHPLC with UV, DAD, RID, and FLD detectors; GC-FID, GC-ECD, GC-MS, ICP-OES, FTIR-UATR, UV-VIS, and GFAAS
  •  Examination of multiresidal impurities and trace pollutants in materials and finished products, such as phthalates, nitrosamines, and volatile organic compounds (VOCs) and other substances mentioned in Annex II of Regulation (CE) 1223/2009
  • Analysis of several residual impurities, including phthalates, pesticides, nitrosamines, and other organic pollutants mentioned in Annex II of EC Regulation No. 1223/2009 in finished goods and raw materials.
  • Metals: examination of inorganic pollutants found in finished goods and raw materials, including Hg, Cd, As, and Pb as well as Ni, Cd, Co, and Cr, which can cause sensitization. Metals important to cosmetics include As, Sb, Cd, Hg, Ni, Co, Cr, Pb, and Cr VI.
  • Release test for the detection of sensitizing metals in cosmetic anhydrous and solid products in fake sweat or saliva; Release test for chemicals or contaminants in medical devices in accordance with ISO 10993-12 in fake sweat or saliva.
  • Accelerated stability testing and stability testing are carried out in climatic chambers under the circumstances outlined in the ICH and PCPC recommendations for chemical, chemico-physical, and microbiological examination.

Contact us today for expedited timelines, reduced
costs and expert support from research to rollout.

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