Solution for Quality Assurance & Quality Control - QualityExpert™
There is an old saying in pharmaceutical industry: “WHAT WAS NOT DOCUMENTED, NEVER HAPPENED”.
Document management is one of the most important parts of GOOD MANUFACTURING PRACTICE (GMP), which is in turn the most important part of Quality Assurance (QA), which guarantees required quality throughout the operations in pharmaceutical industry. With EFFECTIVE DOCUMENT MANAGEMENT in place, the whole field of QA will function ACCORDING TO THE REGULATORY REQUIREMENTS.
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QualityExpert™ brings order and security into a region that used to be the biggest mess and continuous source of frustration to management as well as vulnerable spot at any inspection. |
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QualityExpert™ is part of INFOTEHNA myPharmaExpert Suite™ that deals with all the documentation pertinent to the challenges in GxP environment and covers the following processes:
- Quality Policies and guidelines
- SOP management
- Training management
- Change control
- Supplier management
- CAPA management
- Audits
- Deviations
- Incidents
- Complaints
- Validation
- Records
- And more..
