Executive Development Programme in PharmaTech Serialization Standards

Name: Executive Development Programme in PharmaTech Serialization Standards
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The Executive Development Programme in PharmaTech Serialization Standards is a certificate course designed to empower professionals with the latest knowledge in pharmaceutical serialization. This program emphasizes the importance of implementing traceable and secure systems, complying with global standards, and fighting counterfeit drugs.

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AboutThisCourse

With the pharmaceutical industry's growing demand for experts in serialization, this course offers a timely response to the need for up-to-date skills. It covers essential topics such as coding, data management, and supply chain security, providing a comprehensive understanding of the PharmaTech landscape. By enrolling in this course, learners can expect to enhance their career prospects and contribute to the industry's fight against counterfeit drugs. Through expert-led instruction, practical exercises, and real-world case studies, professionals will gain the skills and confidence necessary to succeed in this critical field.

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CourseDetails

• 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.

CareerPath

Role descriptions: 1. Serialization Engineer: Specialists in implementing serialization standards to ensure regulatory compliance and traceability in the pharma industry. (45%) 2. Validation Engineer: Professionals responsible for verifying and documenting serialization processes' correctness, ensuring compliance and functionality. (25%) 3. Project Manager: Leaders who oversee serialization projects, managing resources, timelines, and stakeholders to achieve successful implementation. (15%) 4. Quality Assurance Specialist: Experts in evaluating and maintaining the quality of serialized products, ensuring compliance with industry standards. (10%) 5. Regulatory Affairs Specialist: Professionals responsible for understanding and navigating regulatory requirements related to serialization standards. (5%)

EntryRequirements

BasicUnderstandingSubject
ProficiencyEnglish
ComputerInternetAccess
BasicComputerSkills
DedicationCompleteCourse

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FastTrack GBP £140

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ThreeFourHoursPerWeek
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StandardMode GBP £90

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TwoThreeHoursPerWeek
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EXECUTIVE DEVELOPMENT PROGRAMME IN PHARMATECH SERIALIZATION STANDARDS

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London College of Foreign Trade (LCFT)

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05 May 2025

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