Disintegration and dissolution testing are critical quality control processes used to evaluate the performance of tablets, capsules, and other solid dosage forms. These tests ensure that pharmaceutical and natural health products (NHPs) release their active ingredients in the appropriate manner and within the required timeframes. Our laboratory utilizes advanced instruments to perform disintegration and dissolution testing, providing accurate and reliable results that support product development and regulatory compliance. These tests are essential for ensuring that products meet quality standards and perform as intended in the body.Disintegration testing evaluates the time it takes for a tablet or capsule to break down into smaller particles in a specified fluid, simulating conditions in the gastrointestinal tract. Dissolution testing measures the rate at which active ingredients are released from a tablet or capsule into a specified fluid, providing information about the product’s bioavailability.
Disintegration and dissolution testing are critical quality control processes used to evaluate the performance of tablets, capsules, and other solid dosage forms. These tests ensure that pharmaceutical and natural health products (NHPs) release their active ingredients in the appropriate manner and within the required timeframes. Our laboratory utilizes advanced instruments to perform disintegration and dissolution testing, providing accurate and reliable results that support product development and regulatory compliance. These tests are essential for ensuring that products meet quality standards and perform as intended in the body.Disintegration testing evaluates the time it takes for a tablet or capsule to break down into smaller particles in a specified fluid, simulating conditions in the gastrointestinal tract. Dissolution testing measures the rate at which active ingredients are released from a tablet or capsule into a specified fluid, providing information about the product’s bioavailability.
Disintegration Test Apparatus: Our laboratory uses state-of-the-art disintegration test instruments that comply with industry standards. These instruments feature precise temperature control, agitation mechanisms, and automated data recording for accurate and reproducible results.
Dissolution Test Apparatus: We employ advanced dissolution testing systems with features such as programmable agitation speeds, temperature control, and automated sampling. These instruments ensure that dissolution testing is conducted under consistent conditions, providing reliable and reproducible results.
Disintegration and dissolution testing are crucial for verifying the performance of pharmaceutical tablets and capsules. These tests ensure that medications release their active ingredients effectively and are absorbed properly in the digestive system. Accurate testing supports drug development, quality control, and compliance with regulatory standards.
For NHPs, disintegration and dissolution testing are used to confirm that dietary supplements and herbal capsules dissolve as intended, releasing their active ingredients effectively. This testing ensures that NHPs meet quality and efficacy standards, and that they are absorbed properly in the body.
In the cannabis industry, dissolution and disintegration testing are essential for ensuring product efficacy and safety. Dissolution testing ensures cannabinoids are released at the correct rate for effective absorption. Disintegration testing verifies that oral dosage forms, like tablets and capsules, break down properly for consistent dosing and bioavailability. Both tests help maintain product quality and regulatory compliance.
Disintegration Test Apparatus: Our laboratory uses state-of-the-art disintegration test instruments that comply with industry standards. These instruments feature precise temperature control, agitation mechanisms, and automated data recording for accurate and reproducible results.
Dissolution Test Apparatus: We employ advanced dissolution testing systems with features such as programmable agitation speeds, temperature control, and automated sampling. These instruments ensure that dissolution testing is conducted under consistent conditions, providing reliable and reproducible results.
Disintegration and dissolution testing are crucial for verifying the performance of pharmaceutical tablets and capsules. These tests ensure that medications release their active ingredients effectively and are absorbed properly in the digestive system. Accurate testing supports drug development, quality control, and compliance with regulatory standards.
For NHPs, disintegration and dissolution testing are used to confirm that dietary supplements and herbal capsules dissolve as intended, releasing their active ingredients effectively. This testing ensures that NHPs meet quality and efficacy standards, and that they are absorbed properly in the body.
In the cannabis industry, dissolution and disintegration testing are essential for ensuring product efficacy and safety. Dissolution testing ensures cannabinoids are released at the correct rate for effective absorption. Disintegration testing verifies that oral dosage forms, like tablets and capsules, break down properly for consistent dosing and bioavailability. Both tests help maintain product quality and regulatory compliance.
Disintegration and dissolution testing are critical quality control processes used to evaluate the performance of tablets, capsules, and other solid dosage forms. These tests ensure that pharmaceutical and natural health products (NHPs) release their active ingredients in the appropriate manner and within the required timeframes. Our laboratory utilizes advanced instruments to perform disintegration and dissolution testing, providing accurate and reliable results that support product development and regulatory compliance. These tests are essential for ensuring that products meet quality standards and perform as intended in the body.Disintegration testing evaluates the time it takes for a tablet or capsule to break down into smaller particles in a specified fluid, simulating conditions in the gastrointestinal tract. Dissolution testing measures the rate at which active ingredients are released from a tablet or capsule into a specified fluid, providing information about the product’s bioavailability.
Disintegration Test Apparatus: Our laboratory uses state-of-the-art disintegration test instruments that comply with industry standards. These instruments feature precise temperature control, agitation mechanisms, and automated data recording for accurate and reproducible results.
Dissolution Test Apparatus: We employ advanced dissolution testing systems with features such as programmable agitation speeds, temperature control, and automated sampling. These instruments ensure that dissolution testing is conducted under consistent conditions, providing reliable and reproducible results.
Disintegration and dissolution testing are crucial for verifying the performance of pharmaceutical tablets and capsules. These tests ensure that medications release their active ingredients effectively and are absorbed properly in the digestive system. Accurate testing supports drug development, quality control, and compliance with regulatory standards.
For NHPs, disintegration and dissolution testing are used to confirm that dietary supplements and herbal capsules dissolve as intended, releasing their active ingredients effectively. This testing ensures that NHPs meet quality and efficacy standards, and that they are absorbed properly in the body.
In the cannabis industry, dissolution and disintegration testing are essential for ensuring product efficacy and safety. Dissolution testing ensures cannabinoids are released at the correct rate for effective absorption. Disintegration testing verifies that oral dosage forms, like tablets and capsules, break down properly for consistent dosing and bioavailability. Both tests help maintain product quality and regulatory compliance.
Disintegration and dissolution testing are critical quality control processes used to evaluate the performance of tablets, capsules, and other solid dosage forms. These tests ensure that pharmaceutical and natural health products (NHPs) release their active ingredients in the appropriate manner and within the required timeframes. Our laboratory utilizes advanced instruments to perform disintegration and dissolution testing, providing accurate and reliable results that support product development and regulatory compliance. These tests are essential for ensuring that products meet quality standards and perform as intended in the body.Disintegration testing evaluates the time it takes for a tablet or capsule to break down into smaller particles in a specified fluid, simulating conditions in the gastrointestinal tract. Dissolution testing measures the rate at which active ingredients are released from a tablet or capsule into a specified fluid, providing information about the product’s bioavailability.
Disintegration Test Apparatus: Our laboratory uses state-of-the-art disintegration test instruments that comply with industry standards. These instruments feature precise temperature control, agitation mechanisms, and automated data recording for accurate and reproducible results.
Dissolution Test Apparatus: We employ advanced dissolution testing systems with features such as programmable agitation speeds, temperature control, and automated sampling. These instruments ensure that dissolution testing is conducted under consistent conditions, providing reliable and reproducible results.
Disintegration and dissolution testing are crucial for verifying the performance of pharmaceutical tablets and capsules. These tests ensure that medications release their active ingredients effectively and are absorbed properly in the digestive system. Accurate testing supports drug development, quality control, and compliance with regulatory standards.
For NHPs, disintegration and dissolution testing are used to confirm that dietary supplements and herbal capsules dissolve as intended, releasing their active ingredients effectively. This testing ensures that NHPs meet quality and efficacy standards, and that they are absorbed properly in the body.
In the cannabis industry, dissolution and disintegration testing are essential for ensuring product efficacy and safety. Dissolution testing ensures cannabinoids are released at the correct rate for effective absorption. Disintegration testing verifies that oral dosage forms, like tablets and capsules, break down properly for consistent dosing and bioavailability. Both tests help maintain product quality and regulatory compliance.
We follow established reference methods to ensure the accuracy and reliability of our disintegration and dissolution testing:
USP <711>: General chapter on Dissolution
USP 〈2040〉: Disintegration and Dissolution of Dietary Supplements
USP 〈1094〉: Dissolution Testing and Related Quality Attributes in capsules
USP 〈701〉: General chapter on Disintegration
EP <2.9.1.> Disintegration of tablets and capsules
EP <2.9.3.> Dissolution test for solid dosage forms
EP <2.9.25.> Dissolution test for medicated chewing gums
Disintegration and dissolution testing are essential for evaluating the performance and quality of tablets, capsules, and other solid dosage forms in the pharmaceutical and natural health product industries. Our laboratory utilizes advanced disintegration and dissolution testing instruments to provide accurate and reliable results, ensuring that your products meet quality standards and regulatory requirements. By adhering to established reference methods and industry guidelines, we support the development and quality control of high-performance products, helping you maintain a competitive edge in the market. Trust our expertise in disintegration and dissolution testing to ensure that your products perform as intended and meet the highest standards of quality and efficacy.
Dissolution testing evaluates how a drug or dietary supplement dissolves in a specific solvent, mimicking the conditions of the digestive system. This process helps determine the rate and extent to which the active ingredients are released from a dosage form, ensuring that they are available for absorption in the body.
Disintegration testing measures how quickly and completely a solid dosage form, such as a tablet or capsule, breaks down into smaller particles under controlled conditions. This test assesses whether the dosage form disintegrates sufficiently to release the active ingredients for absorption.
Both tests are critical for ensuring that your products will perform as intended. Dissolution testing verifies that the active ingredients are released at the appropriate rate, while disintegration testing ensures that the dosage form breaks down correctly. These tests help guarantee product efficacy, safety, and regulatory compliance.
We test a variety of products, including:
Pharmaceuticals: Tablets, capsules, and powders.
Nutraceuticals: Dietary supplements and functional foods.
Biotechnology Products: Innovative formulations and delivery systems.
Dissolution testing evaluates how a drug or dietary supplement dissolves in a specific solvent, mimicking the conditions of the digestive system. This process helps determine the rate and extent to which the active ingredients are released from a dosage form, ensuring that they are available for absorption in the body.
Disintegration testing measures how quickly and completely a solid dosage form, such as a tablet or capsule, breaks down into smaller particles under controlled conditions. This test assesses whether the dosage form disintegrates sufficiently to release the active ingredients for absorption.
Both tests are critical for ensuring that your products will perform as intended. Dissolution testing verifies that the active ingredients are released at the appropriate rate, while disintegration testing ensures that the dosage form breaks down correctly. These tests help guarantee product efficacy, safety, and regulatory compliance.
We test a variety of products, including:
Pharmaceuticals: Tablets, capsules, and powders.
Nutraceuticals: Dietary supplements and functional foods.
Biotechnology Products: Innovative formulations and delivery systems.
Dissolution testing evaluates how a drug or dietary supplement dissolves in a specific solvent, mimicking the conditions of the digestive system. This process helps determine the rate and extent to which the active ingredients are released from a dosage form, ensuring that they are available for absorption in the body.
Disintegration testing measures how quickly and completely a solid dosage form, such as a tablet or capsule, breaks down into smaller particles under controlled conditions. This test assesses whether the dosage form disintegrates sufficiently to release the active ingredients for absorption.
Both tests are critical for ensuring that your products will perform as intended. Dissolution testing verifies that the active ingredients are released at the appropriate rate, while disintegration testing ensures that the dosage form breaks down correctly. These tests help guarantee product efficacy, safety, and regulatory compliance.
We test a variety of products, including:
Pharmaceuticals: Tablets, capsules, and powders.
Nutraceuticals: Dietary supplements and functional foods.
Biotechnology Products: Innovative formulations and delivery systems.
