A well-written procedure documenting the complaint management process, including the creation of a complaint form, is required by the QSR. By Bob Mehta I have always experienced great difficulty in ...

Whether you manufacture a Class I elastic bandage or a Class III deep-brain stimulation device, understanding when to report a medical device complaint is critical and is also required for all FDA ...

The Government Accountability Office has critiqued the Federal Motor Carrier Safety Administration for the use of ambiguous terms and processes used when filing and following up on motor carrier ...

Request To Download Free Sample of This Strategic Report @- The medical device complaint management industry is witnessing a proliferation of mobile apps for complaint resolution due to their ease of ...