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In Topical Formulation Release Testing in India, inconsistent release profiles are often blamed on formulation variability. In practice, part of that variation may originate from the test system itself. For ...

For generic-drug developers, dissolution testing must do more than confirm whether a batch passes a specification. During formulation development, the method should distinguish meaningful changes in composition, process conditions, and ...

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 ...

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 ...

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 ...

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 ...