Quality assurance and QA documentation are areas in which CPPL excels. The team can monitor all documents in a timely manner using the Cyclone Quality Integration Program, ensuring that no linkages are broken and that noncompliances can be managed.
Prior to 2000, every department in the pharmaceutical industry used a different approach to document control. However, with the global quality system evolving and numerous drug regulatory organizations harmonizing their requirements, a lot has changed.
The documentation system is the core of the quality management system, and the quality assurance department has emerged as the hub of the entire industry. A 3600 documentation system was created and launched by Pharma QA in numerous pharmaceutical units. Compared to the standard documentation method, the new system offers numerous advantages.
1. It controls the factory's quality assurance.
2. The degree of modification is minimal.
3. Appropriate management of the documentation.
4. The review procedure is strict.
5. It's simple to trace and archive.
6. The assurance of compliance is provided by the online system and review.
7. Audits grow simpler.
8. Centralized documentation that allows for document issuance and retrieval improves compliance.
9. Cuts personnel and ensures that everyone is responsible for their job duties.