Jul 21, 2017
MDSAP’s Process-Based Audit Approach & Sequence
Jun 22, 2017
CAPA and P&PC: How to Handle These Two Medical Device Compliance Troublemakers
Mar 17, 2017
FDA Proposes Expanding the List of 510(k) Exempt Devices: What You Need to Know
Feb 02, 2017
Case Study: Assembling a Comprehensive Risk Management Approach
Nov 30, 2016
The Medical Device Single Audit Program (MDSAP): What You Need to Know
Sep 29, 2016
The New EU In Vitro Diagnostic (IVD) Regulation: What You Need to Know
