Research Article
Requalification of Friability Testing Apparatus
Author(s): Chethan TP*, Kavya, Abhishek Singh, Rishu Yadav, Laxmi Yadav, Samruddhi Phansekar, Shailendra Gupta and Shubh am Yadav
Re-qualification as a part of validation is the task performed to identify or check that utilities, equipment and ancillary systems can operate within
limits for their intended use. Equipment qualification is a key element in the pharmaceutical quality system. In recent times regulatory agencies are
more focusing on qualification of equipment. Re-qualification of the equipment starts from design of the equipment based on the user requirement
specification and functional requirement specification. The review article provides information on design qualification which is done to identify
whether the proposed design of facilities, system and equipment is suitable for intended purpose, installation qualification which is done to check
whether the equipment is built and installed in compliance with design specification, operational qualification in which the process parameter.. Read More»
DOI:
10.4172/0975-413X.16.1.183-191
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