What is Arena’s Validation Maintenance Service?
Arena’s Validation Maintenance Service (VMS) helps medical device companies subject to FDA regulations and ISO standards reduce the time to validate the Arena application. Arena’s dedicated validation team ensures our solutions are validated against a pre-defined set of customer intended uses.
How does Arena Help?
Arena VMS helps medical device companies control costs and accelerate implementation. VMS reduces or eliminates the need to hire expensive validation resources or divert your team from their daily responsibilities. Arena’s validation team handles validation requirements, impact analysis, planning, along with execution records and corresponding objective evidence — delivered to you for every release with advanced and detailed notifications.
Avoid Being Revision Locked
Validating software can be time consuming and difficult for traditional on-premises solutions, and it often leads customers to avoid upgrades to the latest software release. This creates a situation where you can become “revision locked” to avoid the validation of new features. With our Arena VMS customers, we do the “heavy lifting” for every application release or enhancement.
Arena helps regulated companies validate their Arena application. Everyone involved in the validation process benefits from the validation service.
- Quality and regulatory compliance teams receive quicker validation results.
- Executive stakeholders enjoy faster system implementations, reduced overhead costs, and streamlined compliance.
Arena VMS compresses Arena application validation activities and reduces the work required by your employees to maintain a validated system.
With Arena VMS, you benefit from always having the latest release of Arena software with the minimal amount of work required by your quality and regulatory teams.