Pharmaceutical Cleanroom Commissioning, Certification, and Validation DQ, IQ, OQ, and PQ

TRADELABOR has more than 20 years of experience in the control and treatment of air, working with an experienced and qualified technical staff and with the most advanced technology in this area, which together guarantee the quality of the services provided.

Pharmaceutical products should be manufactured under the requirements of good manufacturing practices by licensed manufacturers with the object of ensuring that users will receive efficacious, safe and good quality products.

Good Manufacturing Practice (GMP):
The overriding principle which governs the quality of every aspect of making a medicine.

„ Every action will only be undertaken by following written instructions and documentation.

„ All facilities and machinery are correct for the purpose and that they, and the environment in which they are situated, is properly cleaned and appropriately treated

„ Raw materials must be stored and handled correctly and that exactly the right materials must be used  at all times.

„ That people, both production workers and support staff, must dress and behave as required, be properly supervised and above all, be trained correctly.

„ That Quality Control is undertaken at every stage of the storage, handling, manufacturing and packing cycle.

 

 

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Continue at:  http://www.gmpua.com/CleanRoom/Qualification/CleanroomQualification.pdf

 

 

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