Compatibility and costumer usability 4. Quality Control (QC) is a system of routine technical activities, to measure and control the quality of the inventory as it is being developed. ASEAN Cosmetic Directive – Testing Requirements. Pharmaceutical quality control testing is usually a matter of repetitive testing of samples of APIs or of a limited number of pharmaceutical products, whereas national quality control laboratories have to be able to deal with a much wider range of pharmaceutical substances and products and, therefore, have to apply a wider variety of test methods. The qualitative and quantitative composition of the substances and materials are described, along with the tests that are to be carried out on the finished and intermediate products as well as on the raw materials. Quality control ensures that the necessary and relevant tests are carried out and that raw materials, packaging materials, and APIs are released for use or sale, only if their quality is satisfactory. This means that all raw materials for the manufacturing of cosmetic products should conform with defined specifications to guarantee a stable level of quality. We conduct on-site inspections , audits , and lab tests to make sure that your beverages are manufactured, stored, and shipped in accordance with your specifications, and meet the safety standards of your destination market. These laboratories have different structures in different countries (central laboratory and district laboratories). Inspecting your product before it leaves the manufacturer’s premises is an effective way of preventing quality problems and supply chain disruptions further down the line. The quality control of cosmetics is important to ensure the efficacy and safety of products and its raw-materials. For quality OIL, FATS and WAXES:- These are used in preparation of creams, lotions, brilliantine, hair oil, lipsticks etc. Quality control is the part of GMP that is concerned with sampling, specifications, testing, documentation, and release procedures. Ion exchange system Distillation Reverse osmosis 2. The critical parameters are for setting standard are:-1. Quality control tests of semisolid products Dr.Maryam kazemi PhD student of pharmaceutics Shiraz university of medical sciences 3 4. Similar concepts apply to bulk drugs. have the highest responsibility for quality control of finished food products. Appendix 2 Challenge test of water miscible cosmetic products. In addition, cosmetic products should be correctly labelled and packaged with appropriate INCI (International Nomenclature for Cosmetic Ingredients) ingredients listing and warnings. For example, wheat quality, after water content, will be tested on the amount and bakery quality of gluten. Lidocaine Ointment • A. Infrared A bsorption Sample: Stir a quantity of Ointment, equivalent to 300 mg of lidocaine, with 20 mL of water, transfer to a separator, and extract with two 30-mL portions of solvent hexane. The standards published within define the legal and scientific foundations for quality control in the development, manufacturing and marketing of pharmaceutical products. Being a key element of quality control, Product Inspections allow you to verify product quality on site at different stages of the production process and prior to its dispatch. The lab-defined range is calculated from QC data collected from testing of normal and abnormal controls. Thus stability and quality of final product is dependent on the purity of water used so pure water should be used in manufacturing of cosmetics. In the different cosmetics regulations worldwide a cosmetic safety assessment for human health is completed for cosmetic products. Similar concepts apply to bulk drugs. These guidelines set out standards for product manufacturing, testing, storage, handling and distribution, to ensure that each step of manufacturing is acceptable for quality and safety of the product. iv Table of Contents Acknowledgements ..... i Dedication ..... ii Abstract ..... iii List of Tables ..... vi List of Figures ..... vii 1. Many manufacturers of plastic granules declare their products to be “compliant with the Pharmacopoeia” or “suitable for pharmaceutical applications”. The bioburden test in general is often seen as the test which is performed on the bulk solution used for parenteral products, either manufactured aseptically or terminally sterilized. Quality control of raw materials and active Ingredients Analysis for the cosmetics industry The quality of cosmetic products is significantly determined by the quality and goodness of the raw materials used. 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