Document management for regulatory compliance
In a very competitive market, companies must adopt a strong commitment to quality. One of the quality actions involves implementing document management standards for regulatory compliance.
In some sectors, the quality requirement is greater and additional standards must be adopted such as GMP (pharmaceutical sector) and OAS (export sector).
All these standards require companies to have all their internal procedures perfectly defined and generate a large amount of important and abundant documentation for a proper performance.
Often, the development of quality procedures suffers problems such as:
The IN2 document management solution for ISO, GMP and OAS regulatory compliance aims to:
- Increase the capacity of management and control of the processes.
- Reduce times, efforts and simplify processes.
- Increase in the quality of the quality document management process itself.