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What are GMP Practices, and Why is It Important for Your Laboratory?

What are GMP Practices, and Why is It Important for Your Laboratory?

GMP stands for Good Manufacturing Practices.

If you work within a laboratory, you’ve likely heard of GLP and GMP practices. However, do you know exactly what they mean? GMP stands for Good Manufacturing Practices. While the name may evoke industrial settings like factories, GMP affects industries like food production, medical devices and supplies, and pharmaceuticals. In addition to manufacturers, they also concern packagers and processors. Essentially, GMP is a set of very flexible regulations designed to maintain manufactured goods’ quality. They ensure goods are adhered to strict quality testing requirements that range from raw ingredients being used to which labs can then conduct quality control tests. Because manufacturing processes can vary widely from one product to another, the requirements are somewhat open to interpretation to ensure that no manufacturer is ever held back. Read on to learn all about GMP practices in your lab!

What Makes GMP Important?

It is crucial to ensure that drugs are effective and safe for patients. It is a matter of trust and safety. Consistency and waste reduction are achievable by maintaining reliable standards across the manufacturing process. For example, in a company that creates medicines and drugs, poor manufacturing practices can be expensive and dangerous for patients. GMP can help promote cooperation across various states and other countries since each manufacturer has to adhere to specific standards. This will promote innovation and competition. GMP protects consumers and helps ensure the reliability and credibility of manufacturers, along with setting standards for high-quality products. These quality standards, in turn, will help ensure that products made and sold aren’t contaminated and that they are effective, safe, and reliable.

Differences Between GLP and GMP?

While they are both quality assurance systems at their core, there are a few key differences. GLP regulations are also designed to ensure traceability of lab records to help evaluate laboratories and make sure that studies are conducted correctly to ensure the integrity of lab results. GMP regulations set the quality control and assurance processes to help uphold high manufacturing standards.

How do GMP Affect Weighing Devices?

Like GLP, GMP sets some standards for the weighing equipment used in manufacturing and testing processes. The scale or balance has to have traceable measurements to ensure that the operator, the time, the date, and all of the calibration data are verifiable. Also, the accuracy, specificity, sensitivity, and reproducibility of the weighing equipment have to be recorded for evaluation. Scales and balances used in industries under GMP regulations have to conform to norms specific to their field. If you have any more questions about GMP lab practices, give the Lab People a call today!

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This entry was posted on Friday, September 3rd, 2021 at 4:39 pm. Both comments and pings are currently closed.

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