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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, ...
Pharmaceutical Research Equipment with Dual-Speed Control: When Is It Necessary?
Dual-speed control is valuable when a pharmaceutical laboratory needs to evaluate two rotational conditions independently within the same dissolution run. It can improve method development, formulation comparison and compatible parallel ...
In Vitro Release Testing IVRT for Ophthalmic Ointments, Gels and Suspensions
In Vitro Release Testing IVRT for ophthalmic products measures the rate and extent at which an active pharmaceutical ingredient is released from an ointment, gel, or suspension into a receptor ...
Subcutaneous Drug Delivery Research: Simulating the Subcutaneous Tissue Environment In Vitro
Subcutaneous Drug Delivery Research increasingly depends on in vitro models that can reproduce selected conditions around an injection site. These conditions include interstitial fluid composition, temperature, diffusion resistance, membrane transport, ...
Pre-Formulation Research Instruments for Intrinsic Dissolution Rate Testing of APIs
Intrinsic dissolution rate (IDR) testing measures how quickly an active pharmaceutical ingredient dissolves from a defined surface area under controlled temperature, medium, and hydrodynamic conditions. Unlike equilibrium solubility, IDR reflects ...