At Dextrose Technologies Pvt. Ltd., we provide UTM (Universal Testing Machine) services for mechanical characterization of materials through tensile, compression, and flexural testing. UTM testing helps quantify strength, stiffness, ductility, and durability, enabling material selection, batch comparison, product validation, and failure investigations across polymers, composites, metals, and engineered materials (test feasibility depends on specimen geometry and standard followed). Tensile Testing We measure tensile properties such as ultimate tensile strength, yield behavior, elongation, and modulus, supporting performance benchmarking and quality checks. Compression Testing We evaluate compressive strength and deformation behavior for materials used in structural, packaging, and functional applications. Flexural (Bending) Testing We assess flexural strength and flexural modulus to understand resistance to bending loads, especially relevant for plastics, composites, and brittle materials. Mechanical strength and durability assessment We support comparative testing across batches and conditions to evaluate durability trends and performance consistency. Deliverables * Force–displacement and/or stress–strain data (as applicable) * Key mechanical parameters (strength, modulus, elongation, etc.) * Test conditions and specimen details (as provided/standardized) * Summary interpretation for material performance evaluation Get started Share your material type, specimen dimensions/standard (if any), number of samples, and required test (tensile/compression/flexural). We’ll recommend the right setup and reporting format.

At Dextrose Technologies Pvt. Ltd., we provide ICP-MS (Inductively Coupled Plasma – Mass Spectrometry) for ultra-trace elemental analysis and sensitive toxic metal screening. ICP-MS is ideal when you need ppb-level detection, strong selectivity, and multi-element quantification in challenging matrices. We support ICH Q3D-oriented elemental impurity testing for development and QC programs, with scope and limits defined by your product type and regulatory requirement. Ultra-trace elemental analysis We quantify multiple elements at trace and ultra-trace levels with calibration-based reporting and clear units (ppb/ppm or µg/L as required). ICH Q3D-oriented elemental impurity testing We support Q3D-oriented workflows by testing target elemental impurities, documenting method conditions, and reporting results in a structured, review-ready format aligned to your defined specification limits. Toxic metal screening at ppb levels We screen and quantify toxic metals at ppb levels (scope-dependent), helping identify contamination risk in raw materials, intermediates, and finished products. Deliverables * Element-wise concentration table with units and detection notes * Method and sample preparation notes (digestion basis as applicable) * QC checks/calibration summary (as agreed) * Interpretation notes highlighting outliers and trends Get started Share your sample type, matrix details, target element list, and required limits/specification. We’ll recommend the right ICP-MS workflow and reporting format.

At Dextrose Technologies Pvt. Ltd., we provide Quality Control (QC) Testing to support batch release, routine compliance, and in-process control. Our chromatography-based QC services deliver consistent, calibration-based results with clear documentation and regulatory-aligned reporting. We help you reduce batch risk, maintain trendable quality metrics, and move faster through internal QA review. Assay Testing (HPLC / RP-HPLC) Accurate content estimation for APIs, intermediates, and formulations using validated/optimized chromatographic methods and standards-based quantification. Related Substances / Impurity Profiling Separation and monitoring of related substances and impurities to support batch comparison, process control, and product quality assessment. Content Uniformity Testing Testing to evaluate dosage consistency across units with structured reporting for easy review and trending. Residual Solvent Analysis (GC-FID / HS-GCMS) Residual solvent quantification using GC-FID or Headspace GCMS, based on target solvent list, matrix, and required limits (ICH Q3C-oriented where applicable). Volatile Impurity Testing Volatile impurity profiling for troubleshooting and routine QC checks using GC techniques suited to your sample type. System Suitability & Routine QC Analysis System suitability testing (SST) and routine batch analysis with documented acceptance checks and clean reporting. Cleaning Validation Sample Analysis HPLC/GC-based analysis of swab/rinse samples for trace residues to support cleaning validation programs (scope-dependent). Outcome you can expect * Batch release readiness with consistent analytical outputs * Ongoing quality monitoring with trend-ready results * Clear, regulatory-aligned reporting for internal QA and client documentation Get started Share your product type, analyte list, specifications/limits, and sample count. We’ll recommend the most efficient QC

At Dextrose Technologies Pvt. Ltd., we provide microbial load and quality control (QC) testing to help you monitor hygiene, process control, and product quality across research and industrial environments. Our services include Total Aerobic Microbial Count (TAMC), Total Yeast and Mold Count (TYMC), and environmental monitoring for water, surfaces, and air—delivered with clear reporting and documented test conditions. Total Aerobic Microbial Count (TAMC) We quantify overall aerobic bacterial load using validated plate-count approaches, providing CFU-based results to support QC and trending. Total Yeast and Mold Count (TYMC) We quantify yeast and mold load for hygiene monitoring and product/process quality assessment, reported as CFU with observation notes. Environmental and Water Microbial Testing We assess microbial contamination in water and environmental samples (swabs, rinse samples, site samples) to support routine monitoring and troubleshooting. Surface and Air Microbial Monitoring We support microbial monitoring of work areas using surface sampling (swabs/contact plates where applicable) and air monitoring approaches (as per scope), enabling facility hygiene assessment and trend tracking. Deliverables * Results report with CFU counts and sample-wise summary * Method notes (media, incubation conditions, and dilution approach) * Observation notes and trend-ready format for repeated monitoring * Optional: follow-up isolation/identification support if abnormal counts are detected Get started Share your sample type (product/water/swab/air), number of samples, and monitoring frequency. We’ll propose a practical QC testing plan and reporting format.

At Dextrose Technologies Pvt. Ltd., we provide Preservative & Biocidal Efficacy Testing to help validate how well preservatives, disinfectants, and antimicrobial formulations control microbial growth under defined test conditions. These studies support product development, comparative screening, and quality investigations with clear documentation and actionable reporting. Preservative Efficacy Testing (PET / Challenge Test) We perform preservative challenge testing to assess whether a formulation can inhibit or reduce microbial growth over time. Testing is executed using defined organisms/timepoints as per the agreed scope, and results are reported as microbial counts/log reduction trends to support performance evaluation. Disinfectant and Biocide Efficacy Studies We evaluate disinfectants/biocides for microbial reduction under controlled contact time and concentration conditions. Studies can be designed for screening or comparative benchmarking based on your intended use case. Antimicrobial Screening of Formulations We screen formulations to compare antimicrobial performance across versions, preservative systems, or concentration ranges—helping you select the best candidate before larger validation studies. Deliverables * Study plan summary (organisms, inoculum approach, contact time, and timepoints as applicable) * Microbial count results (CFU) and log reduction trends * Interpretation notes and clear pass/fail-style conclusions where applicable to the protocol * Contamination controls and observation notes Get started Share your product type (cosmetic/personal care/pharma/industrial), preservative system, target organisms (if specified), and testing standard or expectation. We’ll recommend the right test design and reporting format.

At Dextrose Technologies Pvt. Ltd., we provide antimicrobial susceptibility and efficacy testing to help researchers and product teams evaluate how bacteria and fungi respond to antimicrobial agents. Our testing supports R&D, comparative screening, formulation development, and quality investigations with controlled study conditions, clear documentation, and decision-ready reporting. Antimicrobial Susceptibility Testing (AST) Disc Diffusion Method: Zone-of-inhibition based screening for comparative susceptibility assessment. MIC Determination: Minimum Inhibitory Concentration to identify the lowest concentration that inhibits visible growth. MBC Determination: Minimum Bactericidal Concentration to assess killing endpoints where required. Time-Kill Assays (Kill Curve Studies) We evaluate antimicrobial effect over time by measuring viability at defined timepoints, enabling comparison of efficacy kinetics across agents or concentrations. Antifungal Susceptibility Testing Susceptibility assessment for fungal isolates against antifungal agents, supporting research and screening objectives. Synergistic and Combination Studies We assess combination effects (additive/synergistic/antagonistic trends) to support optimization of multi-agent strategies and formulations. Deliverables Results summary (AST/MIC/MBC/time-kill outputs as applicable) Data tables and interpretation notes aligned to your objective Clear documentation of test conditions and sample identifiers Note: Testing is intended for laboratory, research, and quality purposes. Clinical decisions should be made only by qualified healthcare professionals.

At Dextrose Technologies Pvt. Ltd., we provide HPLC (High Performance Liquid Chromatography) testing for accurate quantification, purity assessment, and impurity profiling across pharmaceutical, biotech, chemical, food, and research samples. HPLC is a reliable, routine-ready technique for separating complex mixtures and generating consistent, calibration-based results for QC and R&D decisions. What HPLC is ideal for * Assay / content estimation of target compounds * Purity testing and impurity profiling * Stability studies and degradation monitoring * Method development and optimization based on analyte and matrix * Batch-to-batch comparison and troubleshooting support Our HPLC workflow Sample understanding + method selection (isocratic/gradient as required) Sample preparation and filtration to protect the column and improve reproducibility Chromatographic separation with optimized conditions (column, mobile phase, flow, wavelength) Quantification using standards and calibration (single/multi-level as needed) Reporting with chromatograms, peak tables, and clear conclusions Deliverables * Chromatograms and peak table (RT/area/area%) * Quantitative results (%, mg/mL, ppm—based on requirement) * Method details and observations (system suitability notes where applicable) * Optional: recommendations for LCMS confirmation for unknown peaks Get started Share your sample type, target analyte(s), expected range, and reporting requirement—we’ll recommend the fastest, most reliable HPLC approach.

At Dextrose Technologies Pvt. Ltd., we provide LCMS (LC-MS/MS) bioanalytical testing for accurate identification and quantification of non-volatile, polar, and thermally sensitive compounds across complex sample matrices. LCMS is the preferred technique when GC methods are not suitable, and when you need high sensitivity with strong selectivity for trace-level analytes. What LCMS is ideal for * Targeted quantification of small molecules (ppm/ppb level as required) * Impurity and degradation profiling * Unknown peak investigation (mass-based confirmation) * Metabolite/biomolecule screening (project-dependent scope) * R&D support, troubleshooting, and routine QC testing Our LCMS workflow Sample understanding and method selection (targeted / screening) Sample preparation and cleanup (matrix-appropriate) LC separation with optimized run conditions for resolution and repeatability MS/MS detection for confident confirmation and robust quantification Reporting with clean documentation and clear conclusions Deliverables * Chromatograms and peak table (RT/area/response) * Mass spectra / MS/MS confirmation details (where applicable) * Quantitative results with calibration approach and method notes * Summary interpretation + recommendations for next-step confirmation if needed Get started Share your sample type, target analytes (if known), expected concentration range, and required reporting format—we’ll recommend the most reliable LCMS approach.

At Dextrose Technologies Pvt. Ltd., we offer Headspace GCMS (HS-GCMS) testing for reliable analysis of volatile organic compounds (VOCs) and residual solvents from complex samples. Headspace sampling focuses on the vapor phase above the sample, reducing matrix interference and improving repeatability for volatile testing. HS-GCMS is ideal when you need sensitive detection and confident identification using mass spectral confirmation. What we test using HS-GCMS * Residual solvents in raw materials, intermediates, and finished products (project-specific scope) * VOC profiling and volatile impurity screening * Unknown volatile peak identification using mass spectra * Support for R&D, troubleshooting, and routine QC requirements How the workflow runs Sample review and headspace condition selection (temperature/time/transfer line) GC separation with optimized method conditions for clean resolution MS detection for confident identification and confirmation Reporting with chromatograms, spectra, and clear conclusions Deliverables * Headspace GCMS chromatograms and peak table (RT/area) * Mass spectra for identified peaks (where applicable) * Quant results with calibration details (ppm/ppb or as required) * Summary interpretation and next-step recommendations if needed Why Dextrose Technologies * SOP-driven execution and clean documentation * Suitable for challenging matrices where direct injection is difficult * Service coverage across major Indian cities through streamlined logistics