A Wright Path Inc.

4 employees

A Wright Path navigate and execute the FDA and global regulatory requirements to launch and maintain products into the marketplace.

Basic info

medical equipment manufacturing

Regulatory Strategy; Worldwide Registrations and Approvals

Quality Management System (ISO 13485/ISO 9001/CMDR/European Directives/FDA QSR)

Pre-Market 510(k) Notifications and PMA Submissions

Compliance

Quality Assurance

Professional Services

CE Marking/European Directive

Pre-IDE

2014