What is Lilial Analysis in cosmetic products? Lilial, chemically known as Butylphenyl Methylpropional, is a compound frequently used to create a pleasant scent in cosmetics and personal care products. However, in recent years, some questions have been raised about the effects and safety of this compound on human health. Therefore, Lilial Analysis in cosmetic products has become an important process that manufacturers and consumers should take into account.

Antiviral Activity Tests in Biocidal Products What is a Biocidal Product? Biocidal products are chemicals used to control or destroy harmful organisms (such as bacteria, viruses, fungi). These products have been developed to protect public health, ensure food safety and for use in various industrial applications. Why Are Antiviral Activity Tests Important? Antiviral effectiveness tests are performed to determine how effective biocidal products are against viruses. These tests are critical to ensuring the product's safety, effectiveness, and compliance with regulatory standards.

Biocontamination is an important issue that needs to be taken seriously, especially in health and safety sensitive environments. In this context, the TS EN 17141 standard is a critical guideline that determines how biocontamination tests should be performed. TS EN 17141 stands out with its applicability in many different sectors, from the healthcare industry to food production, from the pharmaceutical industry to cosmetics. Biocontamination tests not only determine to what extent products and production processes are affected by microorganisms, but also ensure that necessary precautions are taken to control these interactions. TS EN 17141 standard comprehensively addresses the processes of planning, implementing biocontamination tests, evaluating the results and determining control measures.

Gelişen teknoloji ve endüstri ihtiyaçları, laboratuvar hizmetlerini ön planda tutmaktadır. Bilim, teknoloji ve sağlık alanlarındaki gelişmelerin arkasında, doğru ve güvenilir laboratuvar sonuçları vardır. TTS Laboratuvar Hizmetleri, bu alanda lider bir konumda olup müşterilere en üst düzeyde hizmet sunma misyonunu benimsemiştir.

Detergent Residue Test in Cleaning Validation of Medical Products The cleanliness of products used in the medical field is a factor that directly affects the health of patients. Therefore, cleaning validation steps must be carried out in detail and accurately. One of the most critical steps in these validation processes is detergent residue analysis. Detergent residue analysis is used to detect unwanted detergent residues remaining on the surfaces of medical products. The residue left by detergents can impair the functionality of medical devices and equipment and harm users. Therefore, detergent residue analysis plays an extremely vital role. Detergents used during the production of medical devices or during maintenance and sterilization processes should ideally be completely cleaned. But in practice this does not always happen. This is where detergent residue analysis comes into play. Thanks to this analysis, the presence and amount of detergent residues are detected. Detergent residue analysis is a standardized method in cleaning validation processes. Guidelines published by the FDA and other international organizations emphasize the importance of detergent residue analysis for the safety of medical products. Before a medical product is put on the market, it must be tested with detergent residue analysis. Likewise, devices used by hospitals and healthcare institutions should be checked at regular intervals with detergent residue analysis. To summarize, cleaning validation of medical products is a critical process and detergent residue analysis is an integral part of this process. This analysis is performed to guarantee the safety and effectiveness of medical products and devices. Therefore, detergent residue analysis is of great importance for both manufacturers and users.

Asbestos Analysis in TALC Products: Why Is It Critical and How Is It Done? Entrance Talc, or talcum powder, is a natural mineral used in a wide range of applications, from cosmetics and personal care products to food and industrial applications. However, there is concern that talc deposits may be contaminated with asbestos. Asbestos is a type of mineral considered a carcinogen that can cause serious health problems if inhaled or swallowed. This is why asbestos analysis is critical in talc products. Asbestos: Why Is It Dangerous? Asbestos is a fibrous mineral that can cause serious health problems such as mesothelioma and lung cancer. It can also lead to chronic lung diseases such as asbestosis. Asbestos contamination poses a serious health risk, especially since talc products often come in direct contact with the skin or can be inhaled. Regulatory Requirements In many countries, cosmetics and other products containing talc are required to be free of asbestos. Major regulatory authorities such as the FDA (Food and Drug Administration) and the European Union conduct stringent inspections and tests for asbestos-free products. How is Asbestos Analysis Performed? Sample Collection The analysis process begins with a suitable sample collection. This sample should be taken from different parts of the product and mixed homogeneously. Laboratory Tests 1. **Polarized Light Microscopy (PLM)**: This method is usually used in the first step. The sample is examined under a polarized light microscope and the mineral types are determined. 2. **X-Ray Diffraction (XRD)**: This method provides a more detailed analysis and determines the mineral's crystal structure by examining it. 3. **Scanning Electron Microscopy (SEM) or Transmission Electron Microscopy (TEM)**: These methods provide the highest resolution analysis and can even detect asbestos fibers at the nanometer scale. Evaluation According to the test results, the product is either certified as asbestos-free or withdrawn from the market as unsuitable. Conclusion Asbestos analysis in Talc products is a critical step for product safety. This analysis aims to protect users from serious health risks and ensures that the product complies with regulatory standards. A number of laboratory tests are used for asbestos analysis and these tests definitively determine whether the product contains asbestos. We strongly recommend that you work with accredited and reliable laboratories when testing your Talc products.

Total Organic Carbon (TOC) analysis is a method used to measure the amount of organic carbon present in a sample. TOC analysis in medical products is very important for the purity and quality control of the products. This analysis has a very important place especially in products that need to be sterile and of high purity, such as injectable drugs, dialysis solutions, and medical devices. TOC analysis includes the following steps: Sample Preparation The sample usually goes through a sample preparation stage first. This could be, for example, adjusting the pH level, filtering it or bringing it to other predetermined conditions. Oxidation Organic substances are oxidized to carbon dioxide under high temperature and pressure or using an oxidant. Carbon Dioxide Measurement The amount of carbon dioxide formed is usually measured using a conductometric or spectrophotometric detector. Calculation and Interpretation Using the measured amount of carbon dioxide, the total amount of organic carbon in the sample is calculated. The obtained values are compared with acceptable limits for a particular product. Advantages and Disadvantages The advantages of TOC analysis include the ability to obtain fast and reliable results. However, this analysis method only measures the total amount of organic carbon and cannot be used to identify specific organic compounds in the sample. TOC analysis of medical products is usually required by regulatory agencies and must comply with certain standards (eg American Pharmacopoeia, European Pharmacopoeia, etc.). High TOC levels may indicate contamination or contamination of the product, creating potential health risks. Therefore, TOC analysis is a critical quality control step in medical products.