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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