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

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

Compliance

Regulatory Strategy; Worldwide Registrations and Approvals

CE Marking/European Directive

Quality Assurance

Pre-Market 510(k) Notifications and PMA Submissions

Professional Services

Pre-IDE

2014