Latin America’s need for quality medtech keeps the Latin medical device market afloat amid general economic malaise.
Don’t skimp on conducting due diligence.
The expanding international market poses a variety of challenges for medtech companies entering new global territories.
Distribution and installation are extremely important processes that ensure approved, safe, and effective medical devices make it into the hands of healthcare practitioners. In this edition of Devine Guidance (DG), Dr. D continues with his guidance for 21 CFR, Part 820, Subpart – L (Handling, Storage, Distribution, and Installation), specifically 820.160 (Distribution) and 820.170 (Installation).