Keeping standard operating procedures and documentation up to date can be a challenge in the life science sector. Every modification of a process, a simple change in the ways of working, or if a new employee needs to be authorized impacts the quality management system (QMS). To meet Food and Drug Administration (FDA) regulatory requirements, any changes in processes must be documented and easily accessed. An electronic QMS (eQMS) can be the foundation for a life science company and offer quality professionals and the entire organization peace of mind knowing that they have a powerful tool to manage and document business processes for quality, compliance, and product development.
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