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The absolutely programmable Agilent a hundred automatic disintegration apparatus offers a trusted, compliant approach to disintegration testing. The reciprocating push technique, h2o bath, and heater/circulator are included into an individual instrument by using a compact, bench House-preserving style. The apparatus is available in a three-basket design and comes complete with equipment necessary to conduct the typical America Pharmacopeia disintegration test (USP ).
in diameter. A single gap is at the middle, and the other 4 are Similarly spaced in a very circle with a radius of 6 mm
Full disintegration: That state through which any residue of the unit, other than fragments of insoluble coating or capsule shell, remaining on the display screen of your test apparatus or adhering for the decreased surface of the disk, if made use of, is usually a tender mass owning no palpably company Main.
The respective facts is reviewed by lab locale head or his/her designee of that individual lab site.
All testing hardware is completely complemented by Tinius Olsen-created computer software that turns your components into a complicated excellent Examination technique. Be sure you analyze the software items to determine which package deal is true for your application.
Note : Each instrument is calibrated Along with the respective serial variety bath. Tend get more info not to interchange the bathtub.
Our network of laboratories supports you with testing courses that provide an entire array of certification and validation services to meet your distinctive testing requires.
PD action in cables is calculated by attaching the break up-Main HFCT accessory around the cable earth ground. The results are exhibited on the instrument in pico Coulombs (Computer) as numerical values.
With all the very same standard attributes as the opposite DTGi Sequence testers and supporting nearly two basket rack assemblies, the DTG 200i-IS delivers impartial Regulate about Every single test station, making it ideal for the next types of apps:
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It aims to aid the recognition of pharmacopoeial procedures for the disintegration test by regulatory authorities inside the ICH areas. It describes Distinctive requirements for this test being regarded as interchangable to be used within the ICH locations.
Use the designed-in PD classification and interpretation resources to detect difficulties early to prevent hazardous and harmful failures and decrease community downtime/outages
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