CAPA 9 i Software
Product Details
- Long and impressive list of powerful for email alerts, workflow enforcements, and closing conditions.
- Extensive and distinct workflow logic for both nonconformance and CAPA processes.
- Long and impressive list of powerful , many of them exclusive to InfoCAPA 9i.
- Comes with a and with on-site installation/validation documents.
- Regulatory Compliance
- Comply with FDAs GMP/QSR regulations.
- Comply with European Unions Medical Device Directives (MDD).
- Meet the requirements of international quality standards such as ISO 9000 and ISO 13485.
- Track deviant materials
- Investigate and disposition deviant materials
- Initiate corresponding CAPA or other actions to address the nonconformance
- Initiate CAPAs
- Investigate and conduct root cause analysis
- Implement the action identified
- Determine the effectiveness
- Country:South Africa
- telephone:27-603-890-3311
| Long and impressive list of powerful for email alerts, workflow enforcements, and closing conditions |
