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Pharmaceutical Dissolution Testing Services Global Market

In the pharma industry, understanding the dissolution behaviour of drug products is crucial for ensuring their efficacy and safety. At VerGo Pharma Research, located in Goa, India, we specialize in providing comprehensive multiple media dissolution services for a wide range of pharmaceutical formulations. Our expertise in technology transfer enables us to offer tailored solutions that meet the specific needs of our clients.


What Are Multiple Media Dissolution Services?

Multiple media dissolution testing evaluates how a drug releases its active pharmaceutical ingredient (API) in different simulated bodily fluids. This process involves assessing the dissolution profile of a drug product in various media representing different physiological and biorelevant conditions. This approach is essential to meet the requirements of global regulatory bodies, as it helps ensure the drug's consistent performance in diverse conditions.


Our Comprehensive Testing Approach

We employ a rigorous testing methodology to ensure accurate and reliable results:


Diverse Media Selection: We utilize a range of dissolution media, including:
  • Aqueous buffers adjusted to physiological pH levels (e.g., 1.2, 4.5, 6.8, 7.4).
  • Simulated gastric and intestinal fluids, with or without enzymes
  • Surfactant-containing media for poorly soluble drugs.

Advanced Instrumentation: Our laboratory is equipped with state-of-the-art dissolution apparatuses, such as USP Apparatus 1 (Basket) and USP Apparatus 2 (Paddle), ensuring precise and reproducible results.


Method Development and Validation: We develop and validate dissolution methods tailored to each formulation, ensuring compliance with global regulatory standards.

VerGo's Multiple Media Dissolution Services

We offer a complete suite of multiple media dissolution services, including:


Dissolution Method Development: Creating robust and reliable dissolution methods tailored to your specific drug product. This includes selection of appropriate media, apparatus, and testing parameters.


Dissolution Method Validation: Ensuring the accuracy, precision, and reproducibility of the developed dissolution methods, complying with regulatory guidelines.


Routine Dissolution Testing: Conducting routine dissolution tests for quality control and stability studies.


Comparative Dissolution Studies: Comparing the dissolution profiles of different formulations or batches.


Technology Transfer Support: Assisting with the transfer of dissolution methods to other laboratories or manufacturing sites.


Optimize Your Drug’s Performance with Advanced Dissolution Studie

Partner with us to ensure your pharmaceutical formulations meet the highest standards of dissolution performance across multiple media. Contact us today to learn more about our services and how we can support your product development and quality assurance needs.


Applications of Multiple Media Dissolution Testing
  • Oral Solid Dosage Forms (Tablets & Capsules): Determines the dissolution profile across different pH conditions.
  • Poorly Soluble Drugs: Assesses solubility-enhancing strategies like surfactants and complexing agents.
  • Modified-Release Formulations: Ensures proper drug release in targeted regions of the gastrointestinal tract.
  • Biowaiver Studies: Supports regulatory biowaivers for certain formulations based on dissolution data