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Stay informed with Dissolution Tester News, featuring the latest advancements, industry trends, and updates in pharmaceutical testing technology. Discover new features, regulatory changes, and innovative solutions for accurate drug release analysis, ensuring quality and compliance in drug development and manufacturing.
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New Drug Development Tools for Early-Stage Dissolution and Permeation Screening
A new chemical entity may show strong pharmacological activity yet fail because of poor solubility, slow dissolution, rapid precipitation, or limited intestinal permeation. Early-stage screening should therefore examine how much ...
Tablet Disintegration Tester for Large Tablets and Capsules: When Is a Type B Basket Required?
Large tablets and capsules, high doses, nutraceuticals, and oversize capsules can prevent disintegration for testing and cause problems for disintegration testing. Disks, capsules, and nutraceuticals can be too large and ...
Analytical Instrument Manufacturer for High-Throughput Quality Control Laboratories
High-throughput quality control laboratories must analyze exponentially more samples, manage more complex analytical methods, and meet aggressive timelines for delivering accurate results. Simply purchasing more instruments or hiring more analysts ...
Durable Laboratory Instruments in 2026: How to Reduce Total Cost of Ownership
Instrument durability in a laboratory setting means lower total cost of ownership for a variety of reasons, from stability in measurements to decreased unplanned interruptions, and from simplified calibration to ...
Dosage Form Testing in 2026: New Compliance Priorities for Pharmaceutical Laboratories
Pharmaceutical laboratories will discover various unified regulatory changes for dosage form testing in 2026. The greater challenge will be managing the disparate regulatory changes in pharmacopoeias, bioequivalence guidance, dissolution apparatus ...
Lab Equipment Supplier in Asia: China vs. Japan vs. South Korea vs. Singapore
Choosing a Lab Equipment Supplier in Asia requires more than comparing quotations from China, Japan, South Korea, and Singapore. Pharmaceutical laboratories must also evaluate pharmacopoeial compatibility, data integrity, application expertise, ...