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:
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