With 24 years in the Medial Engineering device industry, we dedicate our staff to provide a professional outcome for difficult solutions. We strive to exceed any customer expectations and have expertise in CAPA and 483 resolution. We are experts and seeing and resolving quality issues bottom up and top down. We have direct experience working with government agencies for Medical device submissions (such as the FDA and TUV) answering difficult questions with !00% approval rates.
With an unmatched proven track record our medical engineer expert have successfully produced 100's of Medical Device approvals world wide for design, quality updates, and regulation changes. We are leading experts in the Medical submission and regulatory process. We have lean sigma BB's and love a challenge. We deal with any difficult situation and solve the issue.
Copyright © 2019 Aplusmedicalengineering - All Rights Reserved.