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QMS AND DOCUMENTATION

QMS AND DOCUMENTATION

Documentation is the most crucial activity in Pharmaceutical operations. Under documentation, Quality Management System documents are most important.
The other documentation involves batch documentation, various logs, SOP, procedures, Specification as Methods, etc.
What we do:
1. Support for SOP updating: The SOP will be updating or designing chronologically, guidance based, user-friendly, ease of understanding and as optimal.
2. QMS System Documents :There are various Quality Management System documents including.
* Change Management
* Deviation Management
* CAPA Management
* OOS Management
* Complaint Management
* Risk Management
* Vendor Management
Support and evaluation will be provided by sGMP-PS for effective QMS documentation
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