Ensuring formulation precision with Neopharm.

Neopharm offers Dissolution Testing Services for pharmaceutical products. Our advanced USP Apparatus 1, 2 and 3 dissolution baths comply with all necessary standards, and we use HPLC or UV-Visible to guarantee accurate and dependable outcomes.

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We have services to speed up your product development.

We provide reliable GMP quality control testing and innovative R&D solutions to accelerate product development and improve people's lives.

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We help our clients demonstrate the discriminatory power of dissolution conditions to ensure their formulation quality, efficacy, and performance.


Advanced Technologies for Accurate Results

Our state-of-the-art dissolution bath, coupled with HPLC and UV-Visible enables us to accurately measure and analyze the dissolution profiles of pharmaceutical products. This allows us to assess with precision the release characteristics such as Sink Factor for your active ingredients and the biowaiver of your formulation.

Comprehensive Testing Services

Our dissolution testing services cover a wide range of pharmaceutical products and formulations. Whether you require dissolution testing for immediate-release, extended-release, or delayed-release formulations, we have the expertise and technology to meet your specific needs.

High Quality Data & Reports

We provide you with high quality data and reports which you can use for regulatory submissions. Our reports comply with regulatory requirements such as USP/EP/JP monographs and FDA guidelines.

Neopharm Answers to Common Questions about Dissolution Testing

Dissolution testing is a crucial process in pharmaceutical development and quality control of solid dosage forms. It measures the release rate of the active ingredient, providing information about the drug product dissolution profile and biowaiver.

Dissolution testing provides critical information about the performance, efficacy, and biowaiver of pharmaceutical products. It helps optimize formulation, assess drug release characteristics, ensure consistent product quality, and support regulatory compliance.

Neopharm has capacity to perform dissolution using USP Apparatus 1, 2 and 3 followed by HPLC and UV-Visible testing. These techniques enable accurate measurement and analysis of the dissolution profiles of pharmaceutical products.

Regulatory requirements for dissolution testing vary depending on the specific product and regulatory authorities. Our team is well-versed in these requirements and can guide you in determining the applicable standards for your industry and region.

The duration of dissolution testing depends on various factors such as the specific formulation, the complexity of the product, and the chosen testing method. We strive to provide results within a reasonable timeframe, ensuring efficient and prompt service.

Enhance your pharmaceutical formulations with Neopharm's Dissolution Testing Services. Contact us today to discuss your specific needs and experience the accuracy and reliability of our advanced testing solutions. 

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