Explore our selection of Vankel Dissolution System including USP dissolution apparatus 1, 2, 3, 5, 6, and 7, perfect for pharmaceutical testing. These systems feature interchangeable paddle/basket shaft systems for seamless transitions without height adjustments. We also offer unique accessories to address specific release rate challenges. Find the right Vankel Dissolution System for your needs, available for purchase now!
Vankel Dissolution System
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Question & Answers For:
Vankel Dissolution System
Past Questions, Helpful Answers.
q.
What is a Vankel Dissolution System used for?
a.
A Vankel Dissolution System is used in pharmaceutical testing to measure the rate at which active ingredients dissolve in a solution, ensuring compliance with USP dissolution standards.
q.
What types of dissolution apparatus are included in the Vankel Dissolution System?
a.
The system includes USP dissolution apparatus 1 (Basket), 2 (Paddle), 3 (Reciprocating Cylinder), 5 (Paddle over Disk), 6 (Rotating Cylinder), and 7 (Reciprocating Holder).
q.
Can I switch between different apparatus types easily?
a.
Yes, the system features interchangeable paddle/basket shaft systems that allow seamless transitions without requiring height adjustments.
q.
Does the system support different dissolution testing methods?
a.
Yes, it supports various dissolution testing methods based on the USP standards and can be adapted with unique accessories for specific release rate challenges.
q.
Are accessories available for specialized testing needs?
a.
Yes, unique accessories are available to address specific dissolution challenges and optimize testing for different formulations.
q.
Is the Vankel Dissolution System suitable for all types of pharmaceutical dosage forms?
a.
Yes, it is designed for tablets, capsules, and other solid dosage forms requiring dissolution testing.
q.
Can the system be used for both immediate and extended-release formulations?
a.
Yes, the system is capable of testing both immediate and extended-release formulations to ensure proper dissolution characteristics.
q.
How does this system ensure accurate and consistent results?
a.
The system is designed to meet USP standards, offering precise control over testing parameters such as speed, temperature, and time to ensure reproducibility.
q.
Is the system compliant with regulatory standards?
a.
Yes, it complies with USP, FDA, and other global regulatory requirements for dissolution testing in the pharmaceutical industry.