Dissolution Workstation Software

Agilent Dissolution Workstation Software offers data integrity and automation to analysts using USP dissolution apparatus. Dissolution Workstation Software helps laboratory managers achieve secure and controlled access to methods and dissolution apparatus.

Specific access can be granted to different laboratory analysts with Dissolution Workstation Software. All user changes are tracked and electronically recorded. Secure tracking of what was done, when, and how, with all changes, facilitates 21 CFR Part 11 compliance for the regulated laboratory environment.

Dissolution Workstation Software is ideal for busy laboratory managers responsible for testing drug dosage forms like tablets, gels, capsules, and long-acting injectables. All method parameters, instrument parameters, plus accessory information and test data are captured and recorded.

This Dissolution Software lets you build, edit, search, retrieve, and archive all dissolution apparatus methods and dissolution accessories from a single interface. Laboratories testing generic drugs and branded pharmaceutical products use Dissolution Workstation Software for both efficient operation and data integrity.

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  • Monitor methods in real time, as well as capture and record method parameters, temperature measurements, and sampling times
  • Control of up to four (4) dissolution systems independently from a single PC
  • Track all method/system updates as well as tests performed and store them in easily searchable archives
  • Print, preview, or export documented results generated by a dissolution run in the protected database created locally or on a network
  • Maintain a complete history for all executed tests, which can be digitally verified and electronically signed
  • Integrate or export the data to a laboratory information management system (LIMS) through the client-server architecture
  • Control user rights and privileges by leveraging the security capabilities of the Windows operating system
  • Use with all Agilent dissolution instrumentation
  • Reduce paper trail and manual transcription errors associated with standalone or semi-automated systems
  • Built-in technical controls ensure the security of your data, control access, and facilitate compliance as defined by US FDA 21 CFR Part 11, EU Annex 11 and similar national electronic record regulations




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