Vistaar Standards Management software upgraded for Medical Device Companies


Posted January 24, 2025 by VistaarAI

Vistaar’s new Standards Management Solution offers medical device manufacturers an efficient way to manage global compliance requirements.

 
Vistaar, a leading Regulatory compliance technology solution, announces the upgrade of its comprehensive Standards Management Solution. Predominantly designed to support medical device manufacturers centralize and manage global compliance standards. With a robust standards library and reliable Monitoring, the platform equips companies to ensure compliance with industry Standards.

Highlights of the platform include:

• Centralized Access: One platform for all essential standards, including ISO, IEC, ASTM and ANSI, eliminating the need for multiple sources.
• Real-Time Updates: Automated alerts for the latest revisions and changes in regulatory standards.
• Collaboration Features: Simplified team workflows for document sharing, editing, and approval processes. Also included is Impact Assessment functionality to assess change management necessity.

“Countries requiring diverse Standards compliance, medical device companies need a simpler fit-for-purpose Compliance solution without complicated the process or making it expensive,” said Mahesh Malneedi, CTO at Vistaar. “Our Standards Management Solution ensures that organizations stay compliant while improving efficiency and reducing operational risks while keeping costs as Bay.”

To explore how Vistaar can support your compliance needs, visit https://www.vistaar.ai/standards-management-solution/.
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Contact Email [email protected]
Issued By Vistaar
Phone (877) 877-1519
Business Address 4 Independence Way, Suite 110, Princeton, NJ 08540
Country United States
Categories Medical , Software , Technology
Tags standards management , medical devices , iso standards , iec compliance , ansi regulations , medical device compliance , regulatory compliance , document repository
Last Updated January 24, 2025