ISO 13485 Quality Management System Assessment for medical device manufacturers and specification developers ISO 13485 is the International standard for medical device quality management systems. ISOplan USA can audit your quality management practices, focusing on your medical device design,
Isoplan is a medical device consulting firm with offices in USA and Europe, which offers the following FDA consulting services: FDA Registration and Medical Device Listing FDA Clearance Consulting for Medical Devices US FDA Agent for Medical Device Companies FDA Regulatory Consulting FDA
Isoplan USA has the expertise and knowledge to assist you in: Anesthesia FDA Approval FDA Clearance for Cardiovascular Products FDA Approval for Combination Products Cosmetic/Plastic Surgery Products FDA Clearance Dental Equipment FDA Approval FDA Approval for Disposables FDA Clearance for