Storage Condition for Different Areas in Pharmaceuticals

Standard Operating Procedure of Storage Condition for Different Areas in Pharmaceuticals is describe in this post.

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1. Purpose:

1.1. The purpose is to define storage conditions in different areas for storage of different 

       Areas.

2. Scope:

 2.1. This procedure is applicable to all materials and products being processed at Pharmaceuticals.

3. Responsibilities:

3.1. Quality Assurance Manager

3.2. Quality Control Manager

3.3. QA Officer

3.4. Area Incharge

4. Procedure:

4.1.1. Storage conditions for different areas are as under:


S. #

Area

Storage Conditions

Remarks

Temp.

R/H

1

Raw Material Store

NMT 25 0C ± 20C

NMT50 % ± 5%

 

2

Dispensing of Raw Material

NMT 25 0C ± 20C

NMT50 % ± 5%

 

3

Packing Material Store

NMT 25 0C ± 20C

NMT50 % ± 5%

 

4

Finished Goods Store

NMT 25 0C ± 20C

NMT50 % ± 5%

 

5

In-Process Quarantines of Production

NMT 25 0C ± 20C

NMT50 % ± 5%

 

6

Manufacturing Areas of OSD

NMT 25 0C ± 50C

NMT50 % ± 5%

 

7

Manufacturing Areas of Sachet.

NMT 25 0C ± 50C

NMT50 % ± 5%

 

8

Manufacturing Areas of Liquid Syrup/ Oral Solutions.

NMT 25 0C ± 50C

NMT50 % ± 5%

 

9

Retain Samples Room

NMT 25 0C ± 50C

NMT50 % ± 5%

 


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