NABL Accredited · Thermal Analysis Laboratory

TGA Analysis Laboratory India | Thermogravimetric Analysis Services | NABL

TGA analysis (Thermogravimetric Analysis) services from an NABL-accredited pharmaceutical testing laboratory in India.

TGA analysis — Thermogravimetric Analysis — is an essential thermal characterisation technique for pharmaceutical development and quality control, measuring the precise mass changes that occur in a substance as temperature increases under controlled atmospheric conditions. Auriga Research operates an NABL-accredited TGA analysis laboratory equipped with high-sensitivity microbalance instrumentation capable of detecting mass changes as small as 0.1 micrograms, providing pharmaceutical manufacturers, API producers, and formulation scientists with the thermal decomposition, moisture content, and compositional data they need for regulatory submissions and process optimisation.

The TGA full form — Thermogravimetric Analysis — describes a technique where a sample is heated at a controlled rate (typically 10 C/min) from ambient temperature up to 1000 C while a precision microbalance continuously records the sample mass. Weight loss events correspond to specific thermal processes: evaporation of moisture and residual solvents below 150 C, desolvation of crystalline solvates between 100-250 C, decomposition of organic material above 200 C, and oxidation or reduction events depending on the atmosphere used. Our TGA instruments operate under inert (nitrogen, argon) or oxidative (air, oxygen) atmospheres to characterise these events under different conditions.

Pharmaceutical applications of TGA analysis include determining residual solvent content in APIs per ICH Q3C, quantifying bound and unbound moisture in hygroscopic materials, establishing the thermal stability window for processing and formulation, characterising polymorphic forms that differ in solvation state, and evaluating the composition of multi-component systems such as coated tablets or polymer-drug composites. When combined with DSC analysis, TGA provides a complete thermal fingerprint that supports polymorph screening, stability assessment, and regulatory dossier compilation.

TGA Analysis Capabilities

  • Thermogravimetric analysis from ambient to 1000 C under nitrogen, air, or oxygen atmospheres
  • Residual moisture and solvent content determination for APIs and excipients
  • Thermal decomposition temperature and onset determination
  • Compositional analysis of multi-component pharmaceutical formulations
  • Solvate and hydrate characterisation — stoichiometric water/solvent quantification
  • Ash content and inorganic residue determination
  • Derivative thermogravimetry (DTG) for resolution of overlapping weight-loss events
  • Combined TGA-DSC simultaneous thermal analysis (STA)
  • Isothermal TGA for kinetic stability studies at defined temperatures

Turnaround Time

Standard TGA Analysis: 5-7 business days
Rush TGA Analysis: 2-3 business days
Combined TGA + DSC Package: 7-10 business days
Full Thermal Characterisation: 10-14 business days

Who Needs TGA Analysis

  • API manufacturers requiring thermal stability data and residual solvent quantification per ICH Q3C
  • Formulation scientists characterising drug-excipient compatibility and thermal processing windows
  • Polymorphism screening programmes requiring solvate/hydrate identification and quantification
  • Quality control laboratories needing moisture and volatile content determination
  • Regulatory affairs teams compiling solid-state characterisation data for CTD Module 3

Frequently Asked Questions — TGA Analysis

What is TGA analysis and what does TGA stand for in pharma?
TGA stands for Thermogravimetric Analysis. It is a thermal analysis technique that measures the change in mass of a pharmaceutical substance as a function of temperature or time under a controlled atmosphere. In pharma, TGA analysis is used to determine moisture content, volatile residues, thermal decomposition temperatures, and the composition of multi-component formulations. The technique heats a sample from ambient temperature up to 1000 C while continuously recording weight changes, providing precise data on thermal stability, desolvation, and degradation behaviour.
What is the full form of TGA in pharmaceutical analysis?
The full form of TGA in pharma is Thermogravimetric Analysis. It is also referred to as thermogravimetry (TG). The technique belongs to the thermal analysis family alongside DSC (Differential Scanning Calorimetry) and DTA (Differential Thermal Analysis). TGA specifically measures mass changes, making it complementary to DSC which measures heat flow. Together, TGA and DSC provide a comprehensive thermal characterisation profile for pharmaceutical substances, excipients, and formulations.
What types of pharmaceutical samples can be analysed by TGA?
TGA analysis is applicable to a wide range of pharmaceutical samples including active pharmaceutical ingredients (APIs), excipients, polymeric materials, coatings, drug-excipient mixtures, and finished dosage forms. Common applications include determining residual solvent content in APIs, quantifying moisture in hygroscopic excipients, evaluating thermal stability of heat-sensitive compounds, characterising polymorphic transitions involving desolvation, and assessing the composition of multi-layer tablet coatings. The technique works with solid samples typically requiring only 5-15 mg of material.
How does TGA differ from DSC analysis?
TGA measures mass changes as a function of temperature, while DSC measures heat flow (energy changes). TGA detects events involving mass loss or gain — evaporation, decomposition, oxidation, desorption — but cannot detect events that occur without mass change, such as melting or glass transitions. DSC detects all thermal events including melting, crystallisation, glass transition, and polymorphic transitions. For complete pharmaceutical characterisation, TGA and DSC are typically performed together to correlate mass-loss events with corresponding thermal transitions.
What is the typical turnaround time for TGA analysis?
Standard TGA analysis at Auriga Research is completed within 5-7 business days from sample receipt. This includes sample preparation, TGA measurement under the specified temperature programme and atmosphere, data analysis, and report generation. Rush services are available within 2-3 business days for urgent characterisation needs. Combined TGA-DSC analysis packages are completed within 7-10 business days.

Need TGA Analysis for Your Pharmaceutical Samples?

NABL-accredited thermogravimetric analysis with 5-7 day turnaround. Detailed thermal characterisation reports for regulatory submissions.

Call Now Get a Quote

Type to search services, tests, and locations…