Since 1974 we have been assisting pharmaceutical and medical device companies expedite their applications for marketing approvals and clearances from the FDA and from other international regulatory agencies.
We also assist drug and medical device companies install, manage and maintain quality and manufacturing systems to achieve sustained compliance with FDA, ISO and EU regulations.
We have built a solid reputation developing and implementing strategic and operational plans while successfully assisting more than 500 companies worldwide.
The Shotwell & Carr team: precise, professional, flexible, expert, dedicated to client success.
