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 ICP-OES (Inductively Coupled Plasma – Optical Emission Spectroscopy) for reliable multi-element quantitative analysis across raw materials, intermediates, and finished products. ICP-OES is well suited for routine elemental profiling and screening where you need accurate concentrations across multiple metals and minerals in a single run (scope depends on matrix and required limits). Multi-Element Quantitative Analysis We quantify multiple elements in one method, generating concentration results in clear units (ppm/ppb or mg/L as required) with calibration-based reporting. Heavy Metal and Elemental Impurity Screening We support screening for heavy metals and elemental impurities to help identify contamination risks, support QC decisions, and enable batch comparison. (For ICH Q3D-aligned programs, scope and limits are finalized based on your requirements and standards provided.) Raw Material and Finished Product Analysis We analyze a wide range of matrices—raw materials, powders, liquids, digests, and finished products—based on suitable sample preparation and digestion approach. Deliverables * Results table with element-wise concentrations * Method notes (sample prep/digestion basis as applicable) * Calibration approach and QC checks (as agreed) * Summary interpretation and flags for outliers/trends Get started Share your sample type, target element list, required limits, and reporting units. We’ll recommend the right ICP-OES workflow and sample preparation plan.

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 offer Atomic Absorption Spectroscopy (AAS) for accurate, targeted metal quantification in APIs, excipients, formulations, and raw materials. AAS is well suited when you need focused testing of specific metals with dependable calibration-based reporting. We support heavy metal testing and routine elemental checks for quality, troubleshooting, and compliance-focused workflows (scope and limits defined by your requirement). Targeted metal quantification We quantify selected metals based on your target list and matrix, with results reported in clear units (ppm/ppb or mg/L as required). Heavy metal testing in APIs, excipients, and formulations We test for heavy metals in pharmaceutical and formulation samples to support QC decisions and risk evaluation, with clean documentation and structured reporting. Deliverables * Metal-wise concentration results with units * Method notes and sample preparation basis (as applicable) * Calibration approach and QC checks (as agreed) * Summary interpretation highlighting any outliers Get started Share your sample type, target metal list, required limits, and reporting units. We’ll recommend the most suitable AAS workflow.

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

At Dextrose Technologies Pvt. Ltd., we provide GC-FID (Gas Chromatography–Flame Ionization Detector) testing for accurate, repeatable quantification of volatile organic compounds (VOCs) and residual solvents. GC-FID is ideal for routine solvent profiling and batch release support because it delivers stable responses for many organic compounds and supports precise calibration-based reporting. What we use GC-FID for * Residual solvent testing for raw materials, intermediates, and finished products (as per project requirements) * VOC/volatile compounds quantification in industrial, research, and QC samples * Method setup and optimization based on analyte list, matrix, and required limits How the workflow runs Sample review + recommended injection approach (liquid injection / headspace where applicable) Method selection and run conditions optimized for resolution and repeatability Quantification using standards (single/multi-level calibration as needed) Clear reporting with chromatograms, retention times, and concentration results Deliverables * Chromatograms with peak table (RT/area/area%) * Quantitative results (e.g., ppm / % / mg/L as applicable) * Method notes, calibration details, and observation summary * Optional: recommendations for confirmatory GC-MS when identity confirmation is required Why Dextrose Technologies * SOP-driven testing, clean documentation, and decision-ready reports * Practical support for R&D and industrial QC workflows * Pan-India support with service coverage across major cities

At Dextrose Technologies Pvt. Ltd., we provide end-to-end formulation and product development support for pharmaceuticals, nutraceuticals, cosmetics, and research-driven products. Our services are built for early-stage R&D, proof-of-concept development, and pilot-scale readiness, helping you move from concept to a stable, testable prototype with clear documentation. Our Formulation Capabilities Custom formulation development based on client requirements and target product profile Excipient selection and compatibility assessment to reduce instability and performance risk Lab-scale prototype development for rapid iteration and proof-of-concept Optimization of composition, stability, and performance through structured experiments Product Testing & Evaluation Physicochemical characterization of formulations (as applicable to product type) Stability and compatibility studies for shelf-life and robustness insight Performance and comparative testing across formulations/batches Analytical testing support using advanced instrumentation (HPLC/GC/LCMS, particle sizing, thermal, etc. – scope dependent) Documentation & Reporting Technical and development reports with clear conclusions Data interpretation and result summaries for faster decision-making Client-specific report formats for internal R&D and QA review Support documentation for regulatory-style and academic use (scope dependent) Applications Pharmaceutical formulations, nutraceutical products, cosmetic formulations, research prototypes, and specialty chemical products.

At Dextrose Technologies Pvt. Ltd., we provide BET (Brunauer–Emmett–Teller) surface area analysis to quantify specific surface area and evaluate porosity-related properties of powders and porous materials. BET testing is widely used for catalysts, adsorbents, carbon materials, metal oxides, ceramics, and porous solids, helping you correlate surface area and pore structure with performance and batch consistency. Surface area determination We determine specific surface area (m²/g) using gas adsorption methods and provide comparative summaries across batches or processing conditions. Pore size and volume analysis We support pore characterization by reporting pore volume and pore size distribution (as per method scope), useful for adsorption performance, filtration behavior, and material selection. Catalyst, adsorbent, and material evaluation BET helps evaluate catalysts and adsorbents for surface activity, and supports material QC by tracking porosity changes due to synthesis, activation, milling, or heat treatment. Deliverables * BET surface area (m²/g) * Pore volume and pore size distribution (as applicable) * Isotherm plots/data summary and key parameters * Interpretation notes for batch comparison and performance relevance Get started Share your material type, expected surface area range, degassing conditions (if known), and objective (QC, R&D, catalyst/adsorbent evaluation). We’ll recommend the right BET scope 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