Case Study
Monday, September 22
12:20 PM - 12:50 PM
Live in Berlin
Less Details
This session explores how robust serialization and data logger technologies can enhance supply chain visibility and integrity. Attendees will learn how inadequate real-time risk assessment capabilities and environmental factors, such as temperature fluctuations and untested ink durability, can compromise serialized data visibility and product quality. The discussion will highlight innovative solutions, including the integration of predictive analytics and environmental monitoring, to create resilient and compliant track & trace systems that safeguard product integrity from production to delivery. In this session, you will learn how to:
Dedicated, dependable and motivated professional with over 10+ years of experience in Quality Assurance, Quality Control, Training & Development, Pharmacovigilance processes and Regulatory compliance & audits and Medical device sector. Proficient in initiating, investigating, root cause analysis and closure of market complaints within stipulated timelines. Skilled in documentation, verification and approval of Standard Operating Procedure (SOP) or creating new procedures. Sound exposure in process and system inspection/audit to identify non-compliance and improve efficiency. Demonstrated ability to face regulatory audits including MHRA, USFDA, ENVISA, WHO (Local), CDSCO, MCC & NDA – Uganda as well as various Customer audits. Team player with ability to lead a team by example and motivate them to achieve desired objectives.