Minimize Risk 2021 - Continuing to Audit during a Global Pandemic – How to Optimize Effectiveness and Minimize Risk
Topics/Call fo Papers
Internal Audit and Supplier Audits are essential for medical device companies to self-identify and mitigate risks. The COVID19 pandemic has made this important task even more difficult due to travel restrictions.
Continuous Improvement starts with awareness of issues and opportunities. And without an effective internal audit program, management lacks awareness of the issues within their quality system.
Background
Audit process basics
Comparison of on-site vs. remote audit
Speaker:
Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma.
Continuous Improvement starts with awareness of issues and opportunities. And without an effective internal audit program, management lacks awareness of the issues within their quality system.
Background
Audit process basics
Comparison of on-site vs. remote audit
Speaker:
Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma.
Other CFPs
- Best Practices for Deviation Training
- Dealing with and Preventing Leave Abuse under FMLA, ADA and Workers' Comp
- Navigating the Competing Sanctions Regimes
- Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines Training
- GMP Environmental Monitoring for Pharmaceutical Clean Rooms
Last modified: 2021-02-02 22:33:12