OQ PQ kits for analytical instrument qualification

What is v-kit?

v-kit is a unique independent analytical instrument qualification system for the OQ/PQ qualification of HPLC, GC, LCMS, GCMS and tablet dissolution instruments and processes. The system includes a family of products designed to fit all needs, from the smallest lab to the largest organisation.

What does it consist of?

Windows-based software to create and manage qualification protocols, and deliver controlled consistent qualification tests

Traceable chemical reference standards

Standard operating procedures

Logbook

Who can use it?

Suitably trained personnel can use v-kit as a tool to provide instrument qualification in regulated laboratories, such as those inspected by the FDA

What do I need to get started?

You begin with an Initia Starter Pack, which contains the software, standard operating procedures and permissions needed for a complete qualification. There are various types of Starter Pack available, depending upon the technique you want to qualify and the number of qualifications you need to perform each year. You’ll find full details of these in the comparison table. Chemical reference standards are included in all kits except for the ‘lite’ versions.

Starter kits are topped up as needed with Refill Packs – for multiple or single additional tests as required. These include all necessary consumables and extra licences, and can be ordered in any quantity.

What are the benefits of using v-kit?

There are many benefits, including time and cost savings of up to 80%:

v-kit uses one standard approach – regardless of instrument manufacturer, providing the potential of consistent performance across all your equipment on all sites.

v-kit provides the potential for your lab technicians, usual service providers, or equipment users to perform qualifications.

Control – you can define qualification protocols to meet your own requirements

The user-friendly software, SOPs, and reference standards work seamlessly together

Used correctly, v-kit can aid compliance to regulations issued by international authorities such as FDA (USA), MHRA (UK), IMB (Ireland), etc