Encompassing biomedical markets like pharmaceutical, biotech, research, medical devices, and manufacturing, the life sciences market faces strict regulations set forth by the FDA. From tight timelines and regulatory hurdles in scaling from research to production, through hazardous materials and hazardous material delivery systems, safety is a huge concern.
If your critical systems are not fully operational and well maintained, the impact of downtime and oversights recorded in FDA audits may also pose significant problems. With experts in areas, such as life safety monitoring and alarming, trending and data storage, as well as alarm response and documentation, we know everything has an audit trail.
Serving as a single point of accountability, Envise can provide a streamlined route for problem resolution. Using data specific to your facility, our customized solutions can help you manage operational expenditure and meet agreed maintenance goals, while ensuring a safe, efficient, and compliant environment.