Documentation is the key to operating a pharmaceutical company in compliance with
GMP requirements. The system of documentation devised or adopted should
have as its main objective to establish, monitor, and record "quality" for all aspects
of the production and quality control. Several types of documents are needed to
accomplish this. ( As per WHO)
have as its main objective to establish, monitor, and record "quality" for all aspects
of the production and quality control. Several types of documents are needed to
accomplish this. ( As per WHO)
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