Our solutions support pharmaceutical companies in increasing the efficiency of their business processes, in improving quality management, and in accelerating development. Current standards and legalisation such as the following are taken into account:
- 21 Code of Federal Regulations (CFR)
- Medicines Act
- Good Automated Manufacturing Practice (GAMP)
- Good Laboratory Practice (GLP)
- Good Manufacturing Practice (GMP)
- Good Storage Practice (GSP)
- Integrated batch processing across the board
- Differentiation of the quality control status of inventories (quarantined, free, barred)
- Differentiation of access and release dates
- Control tests and stability checks
- Batch reservations at order entry
- Pharmaceutical data such as RPM (Regional Pharma Market), supply pharmacies, differentiation between prescription and non-prescription drugs, Pharma-Central-Number, etc.
Additional wholly integrated solutions for comprehensive business coordination and planning as well as finance and customer loyalty round out the complete package.
More information on >> GUS-OS Solution Offering
