Oasis-Lims: For Quality Control: Quality Assurance: Research & Development
OasisLIMS provides companies with a flexible LIMS functionality and powerful set of tools as add-ons that help you meet the regulatory, manufacturing and Quality Control requirements. It incorporates project management/coordination, support for analytical method development and formulation development, stability testing, regulatory documentation and Quality Assurance. OasisLims allows you to automate lab processes to increase productivity, efficiency and quality in analysis. Helps you to match the dynamic standards of any lab including GLP and US FDA 21CFRPart11. compliant, UK MHRA, TGA, Health Canada, WHO, GAMP 5, ISO 17025, NABL, FDA Ghana.
- Trend analysis
- Stability studies
- Vendor rating and development
- Equipment calibration and columns management
- Reference and working standard management
- Control/Reserve sample management
- Training records maintenance
- Quality control costing
- Market compliant management
- Chemicals/Media/Glassware/Volumetric solutions/regents inventory management
- Trade returns management
- Environment management
- Dissolution profiling
- Computer system validation
CTL, for Commercial Test Laboratories
Sample Management, lab data management, customer management, rate lists, automatic invoicing and accounts
Enterprise Resource Planning.
Business management suite, specifically designed for pharmaceutical manufacturing units to integrate all business areas that helps production managers and analysts to easily implement cGMP including new Schedule M guidelines, WHO GMP. CrisCon forces users to maintain entire documents / records correctly, completely and timely, as per the requirements of new Schedule M. The user company is thus, always in a state of compliance with regulatory requirements.
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