GMP GOOD MANUFACTURING PRACTICES

 


WHAT IS GMP GOOD MANUFACTURING PRACTICES?

Good Manufacturing Practices (GMP, also known as 'cGMP' or 'current Good Manufacturing Practice') is a key part of quality assurance that guarantees that drugs are consistently made and controlled to meet the quality standards needed for their specific use and as outlined in their product specifications.

 

GMP sets standards for both the making and checking of products, and outlines basic steps to make sure that the processes needed for making and testing are clearly defined, proven, checked, and recorded, and that the people, places, and materials used are appropriate for making medicines and biologicals, including vaccines. GMP also includes legal elements, which cover duties related to distribution, outsourcing manufacturing and testing, and handling issues with products and customer complaints. Specific GMP rules for different types of products, like sterile drugs or biological medicines, are included in a set of addendums to the main GMP rules.

Maintained Product Standards. Product Quality Verification: Collaborating with a company that is certified by the WHO as follows ensures that the products adhere to global quality benchmarks. ...

Compliance with Regulations. ...

Improved Appeal in the Market. ...

Affordability. ...

Availability of Specialized Knowledge.

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