E & E Medicals and Consulting

E & E Medicals and consulting helps medical device companies with a host of FDA regulatory and compliance issues. As a full-service Regulatory, Reliability Consulting and sales corporation for medical device, Intro Vitro diagnostic device (IVD), Pharmaceuticals, and product lifecycle, we help companies develop and improve advanced medical devices. E & E Medicals and consulting brings you the most exceptional access to a team of consultants who are very experienced with the U.S Food and Drug Administration (FDA) and healthcare industry. E & E Medicals and consulting has well-established partners in the EU, Asia, and USA. Listed below are some of the services we offer:
Quality is never an accident….
www.eemedicals.com

FDA 510K SUBMISSION, FDA 510(K) DATABASE, FDA 510(K) SUBMISSION CHECKLIST, FDA 510(K) CLEARANCE, FDA 510(K) APPROVAL, FDA 510(K) APPLICATION, FDA 510(K) CONSULTANT, FDA ESTABLISHMENT REGISTRATION, FDA USA AGENT, FDA PREMARKET NOTIFICATION, FDA REGISTRATION, CE MARK APPROVAL, FDA 483 OBSERVATIONS/WARNING, 510(K) PREMARKET NOTIFICATIONS, FDA DRUG & COSMETIC ESTABLISHMENT, FDA UNITED STATES AGENT, FDA 483 OBSERVATIONS, CCC MARK APPROVAL, CE MARK APPROVAL