3. GSP Hdhshshhs uwushhshs ushshehhs.ksbshhs uwhjw.jjsjs isjshhsgsgsgs .isjshhs usushhshs isisiisus. Hsusuus usubs s.ksh usiis s.isusuus ususuusus uwubehe sushhshs jshjfjudid.i eushej is .usjje PDF

Title 3. GSP Hdhshshhs uwushhshs ushshehhs.ksbshhs uwhjw.jjsjs isjshhsgsgsgs .isjshhs usushhshs isisiisus. Hsusuus usubs s.ksh usiis s.isusuus ususuusus uwubehe sushhshs jshjfjudid.i eushej is .usjje
Course Clinical Pharmacology
Institution Harvard University
Pages 10
File Size 96.9 KB
File Type PDF
Total Downloads 108
Total Views 132

Summary

Hdhshshhs uwushhshs ushshehhs.ksbshhs uwhjw.jjsjs isjshhsgsgsgs .isjshhs usushhshs isisiisus. Hsusuus usubs s.ksh usiis s.isusuus ususuusus uwubehe sushhshs jshjfjudid.i eushej is .usjje...


Description

Sto torrage P Prract ctices Pha harma rmaceu ceuti tica cals Good S to ices ffo or P ha rma ceu ti ca ls ฀

Personnel



Premises and facilities.



Storage conditions



Documentation



Receipt.



Stock rotation.



Dispatch and transport.



Returned goods.



Recall.

Personnel ฀ ฀ ฀

Adequate number of qualified personnel. Training. Suitable clothing and garments.

Premises and facilities. ฀

Adequate storage area.



Un-allowed for unauthorized staff.



Mention different areas required.



Dry, clean. Orderly arranged, pallets above the floor.



Written programs for sanitation, pest control.



Cleaning bay before storage.



Quarantine status and marking.



Clean and separate Sampling area.



Rejected, expired, returned and recalled areas.



Narcotics, cold storage, co

in safe areas.

Storage conditions Temperature records. ฀ Temperature mapping. ฀

Calibrated devices. ฀ Normal conditions; 15 – 25 up to 30., no intense light, well ventilated, no odours. ฀ Defined temperature. ฀

documentation Written instruction, records , procedures, handling of expired. ฀ Retest dates. ฀

Delivery, details of goods. ฀ Receipt records. ฀



Clearly labelled containers and preserve the quality.

Receipt ฀

Checking against purchase order and invoice.



Label.



Physical verification. batch and expiration.



Uniformity of containers.



Storage conditions.



Sampling then quarantine.



Release or Reject.

Stock rotation and control ฀ ฀ ฀ ฀

Stock taking and reconciling the records. Investigate discrepancies. FEFO Outdated stock.

Dispatch and transport ฀ ฀ ฀ ฀ ฀ ฀

Transport conditions. Ice bags. Documented action. Adequate protection. Labelled. Retain of records.

Returned ฀ ฀ ฀

Approved procedures and records. Quarantined for quality re-evalution. Destroyed.

Recalled ฀

Clear system for prompt recall of defective or suspected to be defective....


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