MDI Consultants
55 N Blvd
Great Neck NY New York
United States 11021
Great Neck NY New York
United States 11021
Phone:
+1 516 482 9001
Tags:
Medical Life Sciences Regulatory Affairs
Medical and Life Sciences Regulatory Affairs
FDA Consultants | Medical device consultants & pharmaceutical and Food industry consultants | 510(k)Submissions a medical device, 510(k)Submissions, U.S. Agent, CE mark, ISO 9000, FDA, Pharmaceutical and quality assurance, regulatory consulting company and Authorized Agent, Home | About mdi | Services | Industries | News & Information | Partners | Contact | Site Map Why Choose mdi ? Client Testimonials Client list About mdi Services Industries News & Information Partners Contact Site Map Search Help SEE THE NEW INSIGHT REPORT! Click Here Industry News A New Weekly Feature Bringing you the L atest Relevant Industry News. FDA Quality Systems | FDA Regulatory Compliance FDA Clinical Services to the Medical Device, Pharmaceutical and Food industries. mdi Consultants, Inc. A Medical Device Consulting, U.S. Agent, CE mark, ISO, Pharmaceutical and Quality Assurance, Regulatory Consulting company and Authorized Agent Read the New Article for the CCUS No Silver Bullet Complying with the US FDA GMPS In English or Chinese Click Above _________________________ 510(k) submission assistance FDA Trouble Shooting 483 & Warning Letter Responses Quality System Compliance mdi Consultants Inc. is the leading provider of quality assurance, regulatory compliance and clinical services to the Medical Device, Pharmaceutical and Food industries. Since 1978 we have been providing clients the following high-quality and high-value consulting services: FOR THE LATEST INDUSTRY NEWS CLICK HERE mdi Consultants, Inc. signs agreement with CCUS in Beijing. Cick here for story VIDEO TESTIMONIALS FROM OUR CLIENTS CLICK HERE "THE COMPETENCE AND PROFESSIONALISM OF YOUR COMPANY IS UNSURPASSED IN THE INDUSTRY" MARK ROSOFF, PRESIDENT PRESIDENT ROZINN ELECTRONICS FDA UPDATES INTERNET MARKETING & WEB SITE DEVELOPMENT SERVICES FOR MEDICAL DEVICE COMPANIES FDA compliance ? regulatory strategy development, clinical trial development/ management, cGMP compliance, on-site audits, validation (process, software and sterilization) and 510(k)/PMA/ANDA/NDA
