Good Manufacturing Practices in the Drug Industry, Research Paper Example

The business of healthcare is considered to be one of the most crucial industries in the globe today. Considering that the industry serves the market with not just a consumable product, but particular substances that could be used or abused by the users, the industry is expected to be properly regulated to operate under particular limitations. Noted under these particular regulations is the process by which the businesses involved in the industry are rooted within the common goal of providing cure for the different diseases and ailment that are evidently affecting the society at present.

This is the reason why the legal sanctions surrounding the good manufacturing practice (GMP) rules in producing medicines have been established. The sanctions included within this particular regulation aims to monitor the safety and the high quality results of the products released by organizations enjoined in the industry. Such monitoring and evaluation include operations from the point of research, towards the point of material sorting and even towards the end part of producing the medicines and releasing them to the market for distribution and consumption. The main goal is to protect the health status of the society which is the primary stakeholder of the said process.

Some of the basic principles recognized to stand as the foundation of GMP include the assurance for the manufacturing procedures to be clearly defined and specifically controlled under the general rules of the cleanliness of the facility and the reputable condition of those who are handling the production process. Another matter given attention to is the monitoring of the actual process of manufacturing that is handled on each medicine; whereas when there are particular changes that have been imposed, evaluative measures are applied and checking the preliminary release of the final products are assured through quality check.

Every single process is documented. This specific requirement among manufacturers under the direction of GMP is specifically defined to make sure that everything goes down into writing. This will make it easier for investigators or researchers to note if the organization and/or its staff members are following the basic guidelines for safe medicine production. Every information that has been collected and noted are kept and are made easily available when needed. This is to make sure that just in case particular situations arise that cause the safety of the consumers, the right organization would be held responsible and shall be given directives to make sure the same incident would not happen again in the future.

The consuming public deserves the right to be protected especially when it comes to receiving products from organizations that are supposed to seek their safety and their health. This is the reason why drug manufacturers are expected to take note of the role that they are playing in the society as makers of substances that could mean life or death to the people. Their responsibility to make sure that everyone is safe when taking in the products they made takes a social root that should be monitored from the point of research towards the point of creating the medicines thus making sure that their release in the market would be safe and well directed for a better cause in improving public health status. With all the recommended procedures of assurance taken into consideration, it is expected that such safe route to manufacturing medicines would lead to a better state of supporting public health on the part of the health industry around the globe.