Carizma QM is an affordable, secure and easy to use web-based enterprise class solution to cover all aspects of Quality Management process.
Used by both small and large multinational corporations Carizma QM supports a wide range of BioPharma business processes. It scales to your environment and manages all documents typically required by BioPharma companies such as Operating Procedures (SOP, TOP, Work Instructions), Policies) and processes such as change management, training (training records) and corrective and preventive actions (CAPA).
The aim is to manage all key documentation used within the Quality Management System (QMS) by securely storing and implementing workflows that support the constant improvement of your QMS.
Included within the system is a fully featured document management module, which allows users to manage the whole document lifecycle within Carizma QM itself.
- Centralized repository of all QMS documentation
- Flexible workflows to support various typical QA processes (e.g. review, approval, read & understood, etc.)
- Notification of actions
- Easy and straightforward user interface
- Advanced reporting
Carizma QM is a highly affordable Cloud based solution that provides secure collaboration at the document, site, and study levels. Its configurable workflows ensure improved compliance to study parameters and overall quality to support any regulatory audit. With rules based access workflows it supports seamless collaboration between sponsors, CRO’s, business partners and regulatory bodies.