FDA

This webinar will provide an understanding of the organizational hierarchy of FDA and Health Canada

We will discuss human error categories, near root causes and root causes for these events. We will discuss latest trends in human error issues in the industry.

This webinar training will discuss from content development to formats designed for human error reduction due to procedures.

This webinar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle (SDLC).

It’s important to know what to expect during an FDA audit. Before you are scheduled for a Computer System Audit, we recommend that you review our tips and best practices below.

The Webinar will focus on the importance of ensuring that the validation of an FDA-regulated computer system will meet compliance guidelines.

This webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11.