Standard Operating Procedure for Receiving and Storing Packaging Materials

1) Purpose

The purpose of this SOP is to establish a procedure for the proper receipt and storage of packaging materials to ensure their quality and integrity are maintained.

2) Scope

This SOP applies to all packaging materials used in the manufacturing of pharmaceutical products within the facility.

3) Responsibilities

The responsibilities for this SOP are divided among various roles:

3.1 Receiving Personnel:

Responsible for inspecting and documenting incoming packaging materials.

3.2 Warehouse Staff:

Responsible for storing packaging materials in designated areas under appropriate conditions.

3.3 Quality Control (QC) Personnel:

Responsible for sampling and testing packaging materials to ensure compliance with specifications.

3.4 Quality Assurance (QA) Manager:

Responsible for overseeing the receipt and storage processes and ensuring compliance with regulatory requirements.

4) Procedure

4.1 Receipt of Packaging Materials:

4.1.1 Verify the delivery against the purchase order and accompanying documentation.
4.1.2 Inspect the condition of the delivery, including packaging and labeling.
4.1.3 Document the receipt of materials, noting any discrepancies or damage.

4.2 Sampling and Testing:

4.2.1 QC personnel must sample packaging materials according to the sampling plan.
4.2.2 Perform required tests to ensure materials meet specified quality standards.
4.2.3 Document testing results and release materials for use if they meet specifications.

4.3 Storage of Packaging