For years, we've performed root cause analysis with whiteboards, Post-Its & spreadsheets using The 5 Whys, Ishikawa diagrams, FMEA, and DMAIC methodologies. Now, newer technologies have made the RCA discovery process faster and more precise, and support a direct link to CAPAs.
In addition, digitizing the RCA process allows manufacturers to standardize reporting to certification bodies & authorities and even identify other systems, facilities, and processes that can be improved from this decades-old, extremely valuable continuous improvement tool.
In this webinar, we will start by reviewing:
- goals, benefits, and processes for root cause analysis
- leading RCA tools, including strengths and weaknesses of each
Then you will learn:
- How to leverage RCA to inform CAPAs
- Technologies that make it easier to comply with the FDA’s new RCA requirements for standardization and reporting
- A better, faster, more accurate approach to root cause analysis