If you take any kind of medication, you should know what is in that medication. Every consumer should expect that the medications they take are of the highest quality and that they are free of all contaminants. In short, they should be sure that only what is on the label is what is in the actual medication.
Good manufacturing practices in pharmaceutical facilities and the proof that facilities meet the requirements for GMP compliance, are in place to not only help protect consumers but also ensure their expectations are met, no matter the batch of medications they take.
What Are Good Manufacturing Practices?
Good Manufacturing Practices (GMP) is a system that is in place to ensure every drug product is produced consistently and that their quality is controlled and assured according to the set quality standards and expectations.
GMP can apply to many aspects of production in many industries, but the food and pharmaceutical industries are the ones expected to uphold the highest quality standards because they directly affect our health and well-being.
Why is GMP So Important?
GMP is so important because it helps prevent health hazards and saves money. When poor-quality or contaminated medications reach the consumer, they are likely to cause unwanted health effects, and this has to be prevented at all costs.
Also, these medications might not do what they are intended to do or ensure the consumer or patient is treated appropriately and adequately, and this leads to health issues down the line.
Further, poor quality medication might contain toxic substances, chemicals, or unwanted additives that lead to health complications.
Manufacturing and shipping substandard medications waste money for both consumers and the government. For consumers, they have to go for more hospital visits since their conditions will not be adequately addressed. For the government, it might have to cater to patients who have to make more hospital visits.
Ensuring Good Manufacturing Practices Are Followed
To ensure good manufacturing practices are followed, every pharmaceutical manufacturer must have a plan for how the desired product quality will be met, having a process in place to investigate product quality deviations as well as how to ensure good practices are maintained in all manufacturing operations.
Quality control can be built directly into the manufacturing process to eliminate quality issues. This is because quality defects cannot be sorted out once the medications are already finished.
Players in the pharmaceutical industry can show they are following GMP by allowing GMP facility audits. By getting a GMP certificate from a reputable auditing service, those in the pharmaceutical industry can showcase their commitment to ensuring good manufacturing practices are met.
Since all companies in the pharmaceutical industry must show they are following good manufacturing practices, there is a demand for auditors. Those interested in ensuring public safety through high-quality medication manufacture can complete Cfpie’s GMP facility certification program. By completing the program, you can ensure current FDA GMP expectations are met.
Good manufacturing practices in the pharmaceutical industry are essential because they help protect consumers from poor-quality and dangerous medication. All players in the industry must ensure they are meeting the regulatory requirements to help protect consumers from exposure to potentially harmful medication.