Monthly Archives: April 2013

Guidelines for viable & non -viable counts in gmp areas (As per WHO,2011)

Manufacture of sterile pharmaceutical preparations, four grades of clean areas are distinguished as follows: Grade A: The local zone for high-risk operations, e.g. filling and making aseptic connections. Normally such conditions are achieved by using a unidirectional airflow workstation. Unidirectional … Continue reading

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