A detailed understanding of the pharmaceutical packaging process and supply chain is essential for designing an ideal packaging department — a key sector in both the cannabis and pharmaceutical industries. The Pharmaceutical Packaging Training focuses on all critical aspects of packaging processes and systems, along with associated Good Manufacturing Practice (GMP) requirements and pharmaceutical quality system challenges.This training includes the selection of compatible packaging components, pack design, pack security, and the design and control of packaging processes. It also covers the detailed steps of the supply chain to help participants design a packaging department that is fully prepared for regulatory inspection.
Learning Outcomes
After successful completion of this course, students will be:
Able to understand current cleaning and sterile validation regulatory requirements
Benefits of cleaning/sterile validation
Developing sanitation SOPs
Select and implement different types of cleaning/sterile validation approaches
Able to write cleaning/sterile protocols and validation plans
Able to perform a risk analysis
Able to perform continuous cleaning/sterile process improvements
Module 1
Packaging process
Packaging components
Pack Design
Pack Security
Packaging Validation Regulations and Guidelines
Module 2
Packaging Verification and Packaging Validation
Preparing for Packaging Validation
Writing packaging validation protocol
Module 3
Validation Document List
Validation References
Case Study: Writing a packaging validation protocol
Module 4
Validation Report
CAPA
Gap Analysis
Change Controls
Validation recommendations
Who Should Attend
Anyone who wants to become the following should attend this pharmaceutical validation course online webinar:
Validation Specialist / Scientist / Engineer
Validation Associates
Production Personnel
Technical Team Members
Management Teams
Auditors
Validation Assistant
Validation Specialists
Coordinators
Managers
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