Pharmaceutical companies are a large industry that manufacture so many things. They make mostly medicines, among many other things, and they can come in various forms. From tablets to capsules and syrups, these things require some sort of equipment to make. The machinery and apparatus used for this also have standards to follow for making sure that the quantities of substances are at a proper amount.
Tablet compression was once a manual method, but with the development of technology, manufacturers have found a way to automate the process. This makes assembly line production of tablets and the like easier. Tablet punches and dies are popular machines to assist in tooling.
There has been a call to have similar metrics and specifications for all the machines that are being utilized everywhere. If you are the type that take tablets as form of supplement and medication you would be able to tell that they come in different shapes and sizes. Certain ingredients, apart from the powdered concoction of medicine is mixed with fillers and solidifying substances.
Before the automation and assembly line production of tablets was a more manual method involving presses. Tablets are not only for medicine, they can be for anything that can have a powdered form. They have been used for candy and other substances. While there is no one standard that is being followed globally, there are still two metrics most popularly followed by manufacturers.
One of its biggest benefits is for the OEMs or the Original Equipment Manufacturers. The checking up and qualification process for the machinery becomes easier across the industry since there would be a common blueprint for what to follow and what to look for. Not only will the parts be standardized, but consequently also the validation and inspection metrics.
One, there would be no need to have varying metrics and qualification for any operational inspections on the machinery. This can be different from one standard to another since even the smallest difference can mean a lot of change, on a medicinal level. Any fixes and replacements on the machinery parts become easier because the Original Equipment Manufacturers do not need to make different punches and dies that would fit the many standards that are in the industry.
The differences are very small but these minor variations are what makes interchangeability impossible between machines. The punches and dies have to be compatible for them to work properly. This makes the whole tablet making process costly. Pharmaceutical companies would have to have a variety of machines just to follow the set qualifications depending on where they will be selling the product.
Back in the 1990s there was very little interest in the topic of standardization tablet compression machinery. The companies probably did not want to risk losing their own unique advantages against competition. But eventually the Euro ISO ended up being one of the most widely used one in the industry.
As emphasized the differences may be very little but, these can already affect so much in the operations. Really, punches and dies just vary in specs like punch length and rotation. Having these things all the same from one equipment to another can save so much hassle in time and energy involved in production.
Tablet compression was once a manual method, but with the development of technology, manufacturers have found a way to automate the process. This makes assembly line production of tablets and the like easier. Tablet punches and dies are popular machines to assist in tooling.
There has been a call to have similar metrics and specifications for all the machines that are being utilized everywhere. If you are the type that take tablets as form of supplement and medication you would be able to tell that they come in different shapes and sizes. Certain ingredients, apart from the powdered concoction of medicine is mixed with fillers and solidifying substances.
Before the automation and assembly line production of tablets was a more manual method involving presses. Tablets are not only for medicine, they can be for anything that can have a powdered form. They have been used for candy and other substances. While there is no one standard that is being followed globally, there are still two metrics most popularly followed by manufacturers.
One of its biggest benefits is for the OEMs or the Original Equipment Manufacturers. The checking up and qualification process for the machinery becomes easier across the industry since there would be a common blueprint for what to follow and what to look for. Not only will the parts be standardized, but consequently also the validation and inspection metrics.
One, there would be no need to have varying metrics and qualification for any operational inspections on the machinery. This can be different from one standard to another since even the smallest difference can mean a lot of change, on a medicinal level. Any fixes and replacements on the machinery parts become easier because the Original Equipment Manufacturers do not need to make different punches and dies that would fit the many standards that are in the industry.
The differences are very small but these minor variations are what makes interchangeability impossible between machines. The punches and dies have to be compatible for them to work properly. This makes the whole tablet making process costly. Pharmaceutical companies would have to have a variety of machines just to follow the set qualifications depending on where they will be selling the product.
Back in the 1990s there was very little interest in the topic of standardization tablet compression machinery. The companies probably did not want to risk losing their own unique advantages against competition. But eventually the Euro ISO ended up being one of the most widely used one in the industry.
As emphasized the differences may be very little but, these can already affect so much in the operations. Really, punches and dies just vary in specs like punch length and rotation. Having these things all the same from one equipment to another can save so much hassle in time and energy involved in production.
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