The fully integrated Nova-LIMS/Empower CDS interface provides users with the ability to transfer data directly into related Novatek LIMS modules.
By default, the interface can search out and transfer any Empower/Millennium CDS field on demand, and can be completely configured to suit the needs of the client.
Novatek International is known worldwide for leadership in pioneering 21 CFR Part 11 compliant pharmaceutical software solutions for the entire product life cycle of healthcare quality operations. Novatek provides solutions for manufacturing, packaging, and quality assurance and quality control.
Advanced Quality Nova-LIMS applications provide a comprehensive solution that manages a product's life cycle from new product discovery and development, through to commercial production. Nova-LIMS is a 21 CFR Part 11 Compliant long-term solution that ensures you have centralized control and maintenance of all your data handling software solutions. It is comprised of specialized functional modules such as NOVA-LIMS Software system, Environmental Monitoring LIMS Software, Utility Monitoring LIMS Software, Calibration, preventive maintenance and repair LIMS software, Stability LIMS Software Application, Raw Material Analysis LIMS Software, Finished products Analysis LIMS Software, In Process Analysis LIMS Software, CAPA software, Quality System Management software, Training Management Software, Complaint Management Software, Investigation Management Software, Audit Management Software (Internal and external Audit), Document Management System and Content Management Software, Proof reading software, Packaging Component Analyzer, Lateral Flow device Reader software, Clinical Assay Management LIMS software, Validation, Content, Knowledge Management software, Batch Record, Content, Knowledge Management software, Controlled Inventory Management (LIMS, ERP, MES) system, HPLC Columns, GC Columns, Management LIMS system.
NOVA-LIMS may be configured to work either as a modular unit or an integrated LIMS. Furthermore, its applications can interface with any Microsoft compatible software in order to create a complete paperless integration of data.
All our solutions comply with 21 CFR part 11, Annex 11 regulations as well as ICH, Health Canada, FDA, TGA, MHRA, cGMP, GAMP 5 and a host of other policies.
