Life Science companies play a crucial role in enhancing health. Managing strict regulations from authorities like the FDA requires robust tools for quality professionals. Even basic processes can impact the electronic quality management system (eQMS).
Coming to terms with today’s demands
Maintaining current standard operating procedures and documentation can be difficult when using traditional desktop tools like intranets, Excel, file shares, calendars, and paper documents as your eQMS. A modern eQMS should enable workflow tracking for effective management of Corrective Action and Preventive Actions (CAPA).
Without an up to date eQMS, you will most likely struggle with:
1.
Time-consuming management and administration
2.
Ineffective processes and difficulty improving organizational processes and workflows
3.
Lost company insights and business potential
4.
Risk of failing FDA requirements/audits
5.
Falling behind the competition and being completely out of the market