ISO 13485: Medical Device QMS and Auditing Certification

Two four-hour sessions, 6pm - 10pm EST, two consecutive days: ISO 13485 is internationally recognized as the Quality Standard for Medical Devices, as well as Pharmaceutical manufacturing. This standard ensures products are made to strict, exacting requirements for documentation, process control and reporting. Used for design, development, production and service organizations while ensuring compliance and risk management. This training covers the standard and certifies for auditing.