Agilent Technologies Inc. has introduced the 280-DS
mechanical qualification system, an instrument designed for routine
calibration of a dissolution apparatus. The 280-DS accurately measures,
verifies and documents physical parameters established with recently
enhanced mechanical qualification standards, eliminating the need for
visual interpretation of measurements from manual gauges.
Dissolution
is a technique used in the pharmaceutical industry to determine the
rate at which active pharmaceutical ingredients release from solid
dosage forms such as tablets and capsules. The 280-DS Mechanical
Qualification System, with its 280-DS Workstation Software, redefines
dissolution qualification with optical-sensing technology that delivers
virtually hands-free measurements in seconds.
the customers
now have one instrument that supports whichever type of qualification
their dissolution laboratory of Pharmaceutical requires, said Allan
Little, Agilent the director of marketing for dissolution systems. The
280-the DS precisely measures the critical parameters required for
qualification in a fraction of the time it used to take. Efficiency,
time savings, accuracy,All the latest news from the company I.CH MOTION
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and documentation are all realized with this instrument.
The
280-DS Mechanical Qualification System supports traditional and
enhanced qualification methods to meet current Good Manufacturing
Practices (cGMP). Whether the laboratory uses the U.S. Pharmacopeia?The
Verification of Performance Test(PVT) or the U.S. Food and Drug
Administration and American Society for Testing and Materials (ASTM)
Enhanced Mechanical Qualification standards, the 280-DS offers
unprecedented measurement capabilities.