Introduction to ISO 13485
This one hour session will give employees an introduction to using, implementing ISO 13485:2016 and the GMP requirements for use in the Medical Device Industry. We will review what are some of the current requirements, some of the necessary training that employees should have and how to use ISO 13485:2016 and the GMP requirements to […]
ISO 13485 and QSR Effective Implementation
In this seminar we will outline steps needed to meet the ISO 13485:2016 and QSR requirements for the medical industry and what changes are on the horizon. The ISO 13485:2016 requires numerous additional requirements to ISO 9001 that can impact a companies QMS. The seminar is geared to helping employees understand what is needed.
An Introduction to Implementing and Understanding ISO 13485:2016 and GMP/FDA requirements for use in the Medical Device Industry
This one hour session will give employees an introduction to using, implementing ISO 13485:2016 and the GMP requirements for use in the Medical Device Industry. We will review what are some of the current requirements, some of the necessary training that employees should have and how to use ISO 13485:2016 and the GMP requirements to […]
GMP Fundamentals
This webinar is intended to help you get familiar with FDA’s Quality System Regulations (cGMP) for medical devices. GMP covers all aspects of production from the starting materials, premises, and equipment to the training and personal hygiene of staff. Detailed written procedures are essential for each process that could affect the quality of the finished product. […]
SQF Code Updates
Did you know, the scoring system will be different when this is updated is implemented? There are fewer clauses but more requirements. Dedicated practitioners will work to keep audit scores as high as possible. Learn about this and more in the upcoming QSG webinar. A registered SQF Trainer will provide details regarding Edition 9.0 key updates to […]
