Warehouse

Movement of dispensed materials

Movement of dispensed materials

OBJECTIVE

To lay down a procedure of movement of dispensed raw and packing material to the production area.

SCOPE

This SOP is applicable for transferring dispensed raw materials and packing materials to the production area.

RESPONSIBILITY

Stores Officer, QA Officer, Production Supervisor, and Packing Supervisor shall be responsible to follow the procedure mentioned in this SOP.

PROCEDURE

Material, required for a certain batch, is dispensed by the warehouse personnel as per the authorized requisition in  presence of QA and Production personnel.

RAW MATERIAL

The dispensed raw material is labeled, placed in the cage, locked the cage  by QA personnel and key must be kept with QA. It is stored in the dispensed RM hold area.

When Production requires to use the dispensed material, production requests QA for hand over the material to Production. After that QA hand over the key to production and then Production officer receives the material and after cross verification of the weights in presence of QA , transfers it to the  respective area.

PACKING MATERIAL 

The primary packing material must be transferred through the primary packaging  material entry airlock in to the respective primary packing area through the primary packaging  material entry (After dispensing of primary packaging material warehouse personnel live the dispensed material in to the primary packaging  material entry airlock, production operator receive the material with the supervision of production officer. And transfer into the respective primary packaging area)

The secondary packing material must be transferred in to the secondary packing hall or secondary packaging material hold room with the supervision of Packaging supervisor.

The required quantity of printed material, which must be over coded, has to be transferred to the over  printing area, with the supervision of packaging supervisor.

In case of insert which must be required for folding, has to be transferred in to the insert folding area, with the supervision of production officer.

In case of empty bottle which must be required for filling of liquid orals, has to be transferred in to the bottle decartoning area, with the supervision of production officer.

Post and Updates Click Here

Alvina

Alvina is the Author and founder of Guidelinepharma, she is a pharmaceutical professional having more than 20 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, and Nectar life Science Ltd. During his experience, she faces many regulatorily audits i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda, Kenya, Tanzania, Zimbabwe. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube