Case Study
Monday, September 23
03:10 PM - 03:50 PM
Live in Berlin
Less Details
In this presentation, Esra outlines a strategic approach to achieving compliance and audit readiness for Manufacturing in Pharma. She delves into the software setup, system design, regulatory requirements and data integrity. In this session, you will learn:
Results-driven and accomplished professional with over 23 years of expertise in Computer Systems Validation (CSV) and Quality Assurance (QA). Proven track record in orchestrating GxP systems, ensuring regulatory compliance, and driving continuous improvement initiatives. Adept at leading high-performing teams, implementing Agile Methodology, and successfully presenting and defending systems validation during regulatory audits.