Executive Development Programme in PharmaTech Serialization Standards
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⢠PharmaTech Serialization Standards Overview: Understanding the importance and requirements of serialization in the pharmaceutical industry. This unit should cover the basics of serialization, its benefits, and the global standards such as EU FMD, DSCSA, and China SFDA.
⢠Serialization Technologies: An in-depth look at the technologies used in serialization, including 2D data matrix codes, GS1 standards, and hardware and software solutions.
⢠Implementation Strategies: Best practices for implementing serialization standards, including project management, team organization, and risk management.
⢠Data Management and Analytics: Managing and analyzing the large amounts of data generated by serialization, including data integrity, data exchange, and data analytics for business intelligence.
⢠Supply Chain Visibility: Understanding how serialization can improve supply chain visibility, traceability, and security. This unit should cover the role of serialization in anti-counterfeiting and grey market prevention.
⢠Compliance and Regulations: Ensuring compliance with serialization regulations, including reporting and record-keeping requirements, and understanding the consequences of non-compliance.
⢠Case Studies: Real-world examples of successful serialization implementations, including the challenges faced and the solutions implemented. This unit should provide practical insights and best practices for participants.
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