DOQ LIMS
offers GxP relevant laboratories a secure laboratory IT with tablet capability

As a modern software solution, an intuitive user interface is just as important to DOQ as tablet capability. The user only needs a web browser to use it. Secure process management and the use of a modern form structure contribute to employee acceptance and save time resources during implementation. DOQ can be used across multiple locations.
Saving paper contributes to sustainability in the company and reduces costs. The digital data acquisition reduces walking distances, e.g. when stamping and unstamping process times. Non-updated QM specifications are a thing of the past, as all documents are always available from every mobile workstation.

DOQ's integrated form management enables web-based input forms to be created in DOQ that can be used to simulate a wide variety of analysis and workflow processes. You can define input fields that are filled with data manually or via an interface before an electronic signature completes the process. A complete audit trail and the validation check are also part of DOQ.

All data inputs, whether manual or by analytical instruments, during a sample analysis are stored on an MS SQL database. Using the existing evaluation tool, important key figures can be determined either subsequently or already during the sample analysis.
DOQ is able to display all predecessors and successors of any sample within seconds. Tracking and tracing is possible both horizontally and vertically. The automatic generation of the sample analysis as PDF/A, optionally for each individual batch, guarantees the highest possible audit security with regard to the sample history.

DOQ guides your employees safely through sample processing. In contrast to paper processes, you can block digital processes in their sequence at certain points or provide them with a four-eyes principle. This reduces the frequency of errors. The monitoring of maintenance and calibration supports laboratory staff and also reduces sample throughput times.

Developed in the field of medical technology, DOQ meets all basic regulatory requirements for use in pharmacy, biotechnology and medical technology (FDA 21 CFR Part 11, ISO 13485/2016, MDR). The technical validation support during implementation in the company's software modules (e.g. ERP system) also helps with the overall validation. Each DOQ release is delivered again with a complete validation and thus guarantees a permanently lower effort of the QM department.
Thanks to its modern interface architecture and high user acceptance, DOQ can be implemented within just 2 months. We support you with all the necessary training courses and documents you need to go live.
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