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Username Post: Equipment Validation
Anonymous


12-03-02 09:12 AM - Post#14    

Should laboratory equipment undergo validation even if the process is not?
John
John Cuspilich, Sr. Consultant
Posts 229
John
12-04-02 06:19 AM - Post#17    

The validation process is based on your company's current process risk assessments practices and procedures.

However, 'do-diligance' system or process testing, verification or validation makes great business sense.

John Cuspilich
Sincerely,
John F. Cuspilich, Sr. Consultant RA/QA
FDA.COM
The Auditing Group, Inc.
GMP Publications, Inc.
jcuspilich@auditing.com
jcuspilich@fda.com
856-596-2333 - 866-GXPNews

Anonymous


03-08-05 02:14 AM - Post#1531    

dear Mrs jhon
l Am Erol Kabil l work in drug quality control lab. in Pendik Veterinarian Control and rusarc enstitüte l need equipment validation procedur. İf you have Equipment Validation procedur please send me

Best regartts

Erol KABİL
Pendik veteriner Control Araş.Enstitüsü
Pendik İstanbul TURKEY
Email:erol_kabil@yahoo.com


Anonymous


07-20-05 05:56 PM - Post#2232    

Before initiating the Validation, You have to prepare User requirements and specifications to generate Validation protocol(IQ,OQ and PQ).

SIVA
CQA- RANBAXY
Anonymous


10-05-05 05:00 AM - Post#2905    

Hello,
for instrument qualification to begin, should the instrument be already setup?? or can it be started when it comes out of the package? we are using an outside vendor to do this qualification, and I would appreciate your input.

thanks
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