Deadline for class III device registration in Argentina approaches

07/20/2010 | Clinica (subscription required)

Suppliers of class III medical devices, or those of medium risk, in Argentina have until July 30 to re-register their products in compliance with a four-tiered program aimed at synchronizing the country's registration requirements for medical technologies with the Mercosur bloc's rules.

View Full Article in:

Clinica (subscription required)

Published in Brief:

SmartBrief Job Listings for Health Care

Job Title Company Location
Senior Director Medical Affairs
Edwards Lifesciences
Irvine, CA
Senior Scientist - Cell Engineering Group
Pfizer
San Francisco, CA
Medical Director - Physician
Willamette Valley Community Health
Salem, OR
Area Reimbursement Manager (CT, MA, MD, ME, NH, NJ, NY, PA, VT)
SI-BONE, INC
Multiple Locations, SL_Multiple Locations
Medical Director - Physician
Willamette Valley Community Health
Salem, OR