Software For The Pharmaceutical Industry

Single workstations and networked solutions with built-in data integrity.

- 100% scalable 3-layer software architecture with central MS-SQL database
- Powerful framework with device-independent methods that can be used for different instrument types
- Modules extend the basic functionalities with LDAP integration, LIMS export, data trending, and more
- More than 35 drivers for dissolution and physical testing instruments
- Report, check & evaluate data directly in q-doc and sign with electronic signatures
- Easily create complete batch reports and compare batches over time intervals
- Human readable audit trail and product version control for full traceability and compliance
- Fulfills all requirements for implementation of a 21 CFR part 11 compliant system

Your Data. Simply Managed. –
Actively managing your data saves costs and ensures regulatory compliance. Avoid error-prone manual transcription of test results and other time-consuming activities to consolidate test protocols. Depending on your data management requirements, test systems can be operated stand-alone or networked, allowing you to flexibly choose your desired level of integration.

All your data in one place. –
Take full control of your data and manage all your methods, results, and users with q-doc®. Use the same method on different systems, consolidate data from multiple test runs in a single report, and avoid redundant management of users and their passwords.