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As the influx of new products invade the tablet press industry today, tablet manufacturers together with tooling vendors are constantly innovating the tablet compression technology. The article below discusses how the industry uses technology in determining the maximum compression force for tooling equipment.

Nowadays, it is easy to make your own supplements and vitamins. It may sound complex but actually is quite easy and much more affordable than store brought supplements. To make one’s own supplements, all one needs is an empty capsule made of gelatin or K-capsvegetarian, a capsule machine and the herbs or supplements that one wants to add to the mix.

It is time consuming and expensive for tablet manufacturers to inspect tooling equipment. That said, advancements in technology have made in-process inspections easier to carry out. Here we discuss some of the main technological developments that have facilitated an easier and less costly in-process inspection.

An article with bullet points to help you learn how to operate metal detectors and properly clean them.

The chipping occurs when the edges of the tablets break during the press process or during the handling and coating. Find the Causes And Remedies Of Chipping Related To Formulation Are As Follows

The term humidity and relative humidity has been used interchangeably and some people would even think that both of the terms mean the same. Although both may mean measuring the presence of water in the air, the difference lies in the method by which the measurement is taken.

Hygrometers are important devices in the pharmaceutical world as it measures the relative humidity of the atmosphere, which can affect the products during the manufacturing process. The device includes two thermometer – the dry and the wet bulb. The dry bulb remains dry while a cotton wick that is dipped in water surrounds the wet bulb. In the measurement of humidity, the wet bulb plays an important role.

In the pharmaceutical manufacturing process, it is important that blend uniformity be achieved. If there is poor uniformity, the product can be rejected based on weight or punch pressure causing loss of revenue to the your business. In this article we talk about how to overcome this problem.

Manufacturing tablets that have uniform shape, size, thickness and hardness requires that the press punches used be of similar length. This article talks briefly about how one can determine the punch length, correct measurement as well as the effects of wear and tear.

First discovered in 1928 by Alexander Fleming, penicillin is now one of the most common drug used to help cure patients from bacterial infections. The beta lactam ring of the penicillin is the one responsible for the drug’s anti-microbial activity, which many of the antibiotics medicine have.

The pressure differential is the difference of the atmospheric pressure between the production area and its surrounding. It is measured in pascal using the magnetic pressure gauge.

Terminal sterilization is the process of sterilizing sterile pharmaceutical products. Small and volume parenteral after the packing of the final products. This process is important as it ensures the sterility of the product.

Beef contains a variety of nutrients that are necessary for healthy brain function. Iron, zinc, and B vitamins are vital for fetal brain development. They are important for clear thinking, learning skills, and memory throughout all life stages. Those who are deficient in these nutrients later on in life often suffer with dementia, Alzheimer's disease, and cognitive decline.

Blow-Fill-Seal (BFS) technology is a manufacturing technique used to produce small, (0.1mL) and large volume, (>500mL) liquid-filled containers. Originally developed in Europe in the 1930s, it was introduced in the United States in the 1960s, but over the last 20 years it has become more prevalent within the pharmaceutical industry and is now widely considered to be the superior form of aseptic processing by various medicine regulatory agencies including the U.S. Food and Drug Administration (FDA) in the packaging of pharmaceutical and healthcare products.

This is an introduction in to the different techniques and terminologies that are used in the industry. We have split this in to two parts as there is so much to cover.

It covers everything from the types of equipment that is used in tablet and capsule making to the techniques used on these machines.

This the second part of our introduction in to the different techniques and terminologies that are used in the industry. We have split this in to two parts as there is so much to cover.

It covers everything from the types of equipment that is used in tablet and capsule making to the techniques used on these machines.

There are many factors to be considered in the quest for drug quality assurance.These include environmental moisture, stability and packaging solutions.If all of these aspects are addressed throughout the manufacturing and storage processes, the product can be isolated and protected from all possible threats to quality and efficacy.

To reduce friction during processing, lubricants are added to the formulation of drugs in small batches. There are three reasons why pharmaceutical companies use lubricants.