Drug Industry vs. Quality assurance Unit

QA is a good practice in the manufacture of bio, pharmaceutical products, as it is the process of ensuring for integrity of products to meet the regulatory standards for the proposed indication or proposed use. It is a responsibility that guarantees manufacturers meet the requirements of patients in terms of safety, quality, efficacy, strength, stability and reliability.

Drug Industry vs. Quality assurance department The spate of counterfeit, inferior /adulterated medicines is a serious concern in the industry. The biopharma segment interpreted an increase in regulations after the thalidomide disaster in 1957. The rigorous, in-depth, scientific, systematic and sustainable move towards to commercial pharmaceutical manufacturing ensures protection of public health.

The arrangement of specifications and practice control assesses in the industry, easily denoted as standard operating procedures (SOPs) that are formulated by drug regulatory agencies and scientific community to ensure good manufacturing practices (GMP) are in place.

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