Charisma

#	Content
1	Module 1: Introduction to Material Receipt
2	Module 2: Regulatory Requirements
3	Module 3: Receiving Process
4	Module 4: Inspection of Incoming Materials
5	Module 5: Material Identification and Traceability
6	Module 6: Quarantine and Sampling
7	Module 7: Documentation and Record Keeping
8	Module 8: Handling Non-Conforming Materials
9	Module 9: Storage After Receipt
10	Module 10: Inventory Control
11	Module 11: Health, Safety, and Good Warehouse Practices
12	Module 12: Audits and Inspection Readiness
13	Module 13: Practical Workshops and Case Studies

#	Outcomes
	• Explain the material receipt process within a quality management system.
	• Verify supplier documentation and shipment accuracy.
	• Conduct receiving inspections according to approved procedures.
	• Apply material identification and status labeling requirements.
	• Manage quarantine and release processes for incoming materials.
	• Document receiving activities in compliance with GMP documentation practices.
	• Identify and report damaged, expired, or non-conforming materials.
	• Maintain complete material traceability throughout the supply chain.
	• Coordinate effectively with warehouse, procurement, QA, and QC departments.
	• Contribute to inventory accuracy and regulatory compliance.

#	Participants
1	� • Warehouse and Stores personnel
2	� • Warehouse Supervisors and Managers
3	� • Quality Assurance (QA) personnel
4	� • Quality Control (QC) personnel
5	� • Receiving and Logistics personnel
6	� • Procurement and Purchasing staff
7	� • Supply Chain professionals
8	� • Inventory Controllers
9	� • Manufacturing and Production personnel
10	� • Distribution and GDP personnel
11	� • Materials Management staff
12	� • Internal Auditors
13	� • Regulatory Affairs professionals
14	� • Pharmaceutical, Biotechnology, Medical Device, Food, and Healthcare professionals
15	� • Anyone responsible for receiving, handling, or storing incoming materials