EUROLAB
bp-appendix-x-identification-tests-for-organic-compounds
Pharmacopoeia-Based Assays BP Appendix VIII G: Total Ash in Herbal ProductsBP Appendix XI C: Test for Water Insoluble MatterBP Appendix XII C: Uniformity of Weight TestBP Appendix XII F: Microbial Limits for Cosmetic PreparationsBP Appendix XII G: Total Aerobic Microbial Count in LiquidsBP Appendix XIV A: Refractive Index Measurement for OilsBP Appendix XIV C: Determination of pH Using ElectrodesBP Appendix XIV F: Assay of Sulphates by GravimetryBP Appendix XV B: Assay of Chloride in Raw MaterialsEP 2.2.2 UV-Visible Spectrophotometry AssayEP 2.2.20 Thin-Layer Chromatography Identity TestingEP 2.2.24 Absorption Spectrophotometry in the IR RegionEP 2.2.28 Gas Chromatography Method ValidationEP 2.2.3 Potentiometric pH MeasurementEP 2.2.32 Loss on Drying DeterminationEP 2.2.38 Differential Scanning Calorimetry AssayEP 2.4.4 Sulphated Ash for ExcipientsEP 2.4.8 Sulphated Ash AnalysisEP 2.5.12 Water Content (Karl Fischer Method)EP 2.6.12 Microbiological Examination of Non-Sterile ProductsEP 2.6.14 Microbiological Integrity Testing for PackagingEP 2.6.27 Bacterial Endotoxin Test Using Recombinant Factor CEP 2.9.1 Uniformity of Mass for Single-Dose PreparationsEP 2.9.3 Friability Testing for Uncoated TabletsEP 2.9.5 Hardness of Tablets MeasurementEP 2.9.7 Dissolution Testing for Gastro-resistant TabletsJP 3.01 Uniformity of Content in Powdered DrugsJP 3.03 Color and Clarity of Solution TestingJP 3.05 Osmolarity Testing in Ophthalmic SolutionsJP 4.01 Identification of Active Pharmaceutical IngredientsJP 4.04 Assay of Active Compounds Using UV MethodJP 4.05 Water Determination in Raw MaterialsJP 5.02 Determination of Peroxides in Lipophilic CompoundsJP 6.01 Test for Related Substances Using HPLCJP 6.03 Dissolution Test for Capsule Dosage FormsJP 6.04 Analysis of Pesticide Residues in Herbal MedicinesJP 6.05 Testing for Insoluble Matter in InjectionsJP 7.01 Test for pH in Oral SolutionsJP 7.02 Heavy Metal Test for Injection ProductsJP 8.02 Identity Testing Using IR SpectroscopyJP 8.03 Residual Solvents in APIsJP 9.01 Chromatographic Purity for Active SubstancesJP 9.04 Microbial Limits Test for OintmentsUSP <1029> Good Documentation Practices for TestingUSP <1030> Biological Assay for AntibodiesUSP <1032> Design and Conduct of Bioavailability StudiesUSP <1039> Reduced Sampling and Testing Plan JustificationUSP <1047> Testing for Biotechnological Protein ProductsUSP <1058> Analytical Instrument QualificationUSP <1062> Tablet and Capsule Weight Variation StudyUSP <1078> Good Manufacturing Practices for Bulk ExcipientsUSP <1079> Good Storage and Shipping Practices for Drug ProductsUSP <1088> Stability Testing of Drug SubstancesUSP <1092> Tablet Coating Performance TestingUSP <1106> Whole Package Integrity TestingUSP <1111> Microbiological Quality of Nonsterile ProductsUSP <1116> Control of Bioburden in Clean RoomsUSP <1117> Best Practices for Handling Hazardous CompoundsUSP <1163> Quality Assurance in Pharmaceutical CompoundingUSP <1181> Evaluation of Stability-Indicating MethodsUSP <1191> Stability Testing for Compounded PreparationsUSP <1216> Tablet Friability TestingUSP <121> Sterilization Assurance Level TestingUSP <1224> Transfer of Analytical ProceduresUSP <1225> Validation of Analytical ProceduresUSP <1226> Verification of Compendial ProceduresUSP <1227> Validation of Microbial Recovery from Pharm WatersUSP <1228> Depyrogenation Validation of EquipmentUSP <1231> Water for Pharmaceutical Purposes TestingUSP <231> Heavy Metals Limit Test for PharmaceuticalsUSP <232> Elemental Impurities – Limits in Finished ProductsUSP <233> Elemental Impurities – Procedures for AnalysisUSP <39-NF34> Identification Testing of Active Pharmaceutical IngredientsUSP <41> Weights and Balances Calibration CheckUSP <467> Residual Solvents Testing in Drug SubstancesUSP <51> Antimicrobial Effectiveness Testing in Aqueous FormulationsUSP <61> Microbial Enumeration Tests for Raw MaterialsUSP <62> Tests for Specified MicroorganismsUSP <701> Disintegration Test for Uncoated TabletsUSP <711> Dissolution Testing for Immediate-Release Dosage FormsUSP <788> Particulate Matter in Injections AnalysisUSP <800> Hazardous Drugs Handling ValidationUSP <800> Surface Contamination Testing for Hazardous DrugsUSP <857> UV-Visible Spectroscopy System SuitabilityUSP <85> Bacterial Endotoxins Test for Parenteral PreparationsUSP <905> Uniformity of Dosage Units for CapsulesUSP <905> Uniformity of Dosage Units Testing

BP Appendix X: Identification Tests for Organic Compounds Laboratory Testing Service

Provided by Eurolab

Comprehensive Guide to BP Appendix X: Identification Tests for Organic Compounds

Standard-Related Information

The testing service provided by Eurolab for BP Appendix X: Identification Tests for Organic Compounds is governed by various international and national standards. These standards ensure that the test results are accurate, reliable, and compliant with industry requirements.

  • ISO/IEC 17025:2017: General Requirements for the Competence of Testing and Calibration Laboratories

  • ASTM D5766-15: Standard Test Method for Determination of Water in Liquid Hydrocarbons; Petroleum, Distillates, and Miscellaneous Products

  • EN 14110:2003: Chemical analysis - Sampling and preparation of samples - General principles and procedures

  • TSE EN ISO 5667-1:2018: Water quality - Sampling - Part 1: Guidance on the design of sampling programmes

    • These standards are developed by reputable standard development organizations, such as:

  • International Organization for Standardization (ISO)

  • American Society for Testing and Materials (ASTM)

  • European Committee for Standardization (CEN)

    • The evolution of standards is an ongoing process, with new versions being published to reflect changes in technology, industry practices, and regulatory requirements.

    Standard Requirements and Needs

    BP Appendix X: Identification Tests for Organic Compounds testing is a critical requirement for various industries, including:

  • Petroleum industry: Accurate identification of organic compounds is essential for the production, transportation, and storage of petroleum products.

  • Chemical industry: Chemical manufacturers rely on accurate identification of organic compounds to ensure product quality and compliance with regulations.

  • Pharmaceutical industry: Identification of organic compounds is crucial for ensuring product safety and efficacy.

    • The consequences of not performing this test can be severe, including:

  • Accidental contamination or misidentification of products

  • Non-compliance with regulatory requirements

  • Loss of business reputation and customer trust

    • Test Conditions and Methodology

    The testing service provided by Eurolab for BP Appendix X: Identification Tests for Organic Compounds involves the following steps:

    1. Sample preparation: The sample is prepared according to the relevant standard, which may involve grinding, drying, or dissolving the material.

    2. Instrument selection: The appropriate instrument is selected based on the type of organic compound being identified and the sensitivity required.

    3. Measurement and analysis: The measurement and analysis are performed using techniques such as gas chromatography (GC) or liquid chromatography (LC).

    4. Calibration and validation: The instrument is calibrated and validated according to the relevant standard.

    5. Quality control measures: Quality control measures, such as internal standards and blanks, are implemented to ensure the accuracy of the results.

    The testing parameters and conditions for BP Appendix X: Identification Tests for Organic Compounds are specified in the relevant standards.

    Test Reporting and Documentation

    The test results for BP Appendix X: Identification Tests for Organic Compounds are documented and reported according to the following guidelines:

  • Report format: The report is structured according to the relevant standard, which may include information on the sample preparation, measurement and analysis methods, calibration and validation procedures, and quality control measures.

  • Interpretation of test results: The interpretation of test results is performed by trained personnel who are familiar with the relevant standards and industry practices.

  • Certification and accreditation: Eurolabs testing service is accredited according to ISO/IEC 17025:2017, which ensures that the testing laboratory meets the required technical competence.

    • Why This Test Should Be Performed

    The benefits of performing BP Appendix X: Identification Tests for Organic Compounds include:

  • Risk assessment and mitigation: The test helps to identify potential risks associated with organic compounds.

  • Quality assurance and compliance: The test ensures compliance with industry standards and regulations.

  • Competitive advantages: Performing this test demonstrates a commitment to quality and safety, which can improve customer trust and loyalty.

  • Cost savings: The test helps to prevent accidents and environmental damage, which can result in significant cost savings.

    • Why Eurolab Should Provide This Service

    Eurolab is well-positioned to provide the BP Appendix X: Identification Tests for Organic Compounds testing service due to its:

  • Expertise and experience: Eurolab has extensive experience in laboratory testing services, including organic compound identification.

  • State-of-the-art equipment and facilities: Eurolabs laboratories are equipped with modern instruments and equipment that meet international standards.

  • Qualified and certified personnel: Eurolabs technicians and analysts are trained and certified according to relevant standards.

  • Accreditation and certification: Eurolab is accredited by international organizations, such as ISO/IEC 17025:2017.

    • Conclusion

    The BP Appendix X: Identification Tests for Organic Compounds testing service provided by Eurolab is a critical requirement for various industries. The test ensures compliance with industry standards and regulations, prevents accidents and environmental damage, and demonstrates a commitment to quality and safety. By selecting Eurolab as its testing partner, customers can be assured of receiving accurate and reliable results that meet international standards.

    References

  • ISO/IEC 17025:2017 - General Requirements for the Competence of Testing and Calibration Laboratories

  • ASTM D5766-15 - Standard Test Method for Determination of Water in Liquid Hydrocarbons; Petroleum, Distillates, and Miscellaneous Products

  • EN 14110:2003 - Chemical analysis - Sampling and preparation of samples - General principles and procedures

  • TSE EN ISO 5667-1:2018 - Water quality - Sampling - Part 1: Guidance on the design of sampling programmes

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