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Want to eliminate events and predict quality near misses; reduce deviation rate by >90% and gain >25% production efficiency simultaneously?
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Pharmaceutical Regulatory Affairs: Open Access

ISSN: 2167-7689

Open Access

Want to eliminate events & predict quality near misses; reduce deviation rate by >90% & gain >25% production efficiency simultaneously?


5th International Conference and Exhibition on Pharmaceutical Regulatory Affairs

August 03-05, 2015 Orlando, USA

Amy Peterson

Quality Systems, USA

Scientific Tracks Abstracts: Pharmaceut Reg Affairs

Abstract :

Lessons learned from North America Commercial Nuclear: Design the Most Robust & Effective Deviation/CAPA System within the Pharmaceutical Industry, Predict but Monitor Effective Corrective Actions; Implement Quality Near Misses to Generate Preventive Actions, Encompass Adverse Human Error Trends; Utilize Error Prevention Techniques, Achieve Adherence to Standard Operation Procedures (SOP); Learn KEY Role of Human Factoring Processes and Instructions, Manage Human Error in Quality Systems to prevent events.

Biography :

Amy Peterson is QA Manager at Quality Systems, USA.

Email: ncsu7219@gmail.com

Google Scholar citation report
Citations: 533

Pharmaceutical Regulatory Affairs: Open Access received 533 citations as per Google Scholar report

Pharmaceutical Regulatory Affairs: Open Access peer review process verified at publons

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