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: 2019

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Chemical Purity and Its Impact on Manufacturing

Since its inception, chemical science has evolved from back-room apothecaries and botanicals to a full-fledged industry employing nearly 810,000 people, including in the pharmaceutical sector. As humans have gotten a better handle on the science of medicine, manufacturing standards have had to rise to keep up with them. When consumers take pills for medicinal purposes,...

3 Signs And Symptoms That Your Fume Hood Needs To Be Replaced

The U.S. alone possesses over 45% of the global pharmaceutical market. We are able to exercise such power and control thanks to our dedication to precision; our GMP quality control and clean room standards allow us to ensure that our pharmaceutical products are safe to use and of excellent quality. Though there are many factors...

What Are The Biggest Contamination Risks In A Clean Room?

The U.S. is the number one largest national producer of chemical products globally. We have achieved this prestigious position as a result of our dedication to clean room standards and chemical purity; if we were unable to guarantee the quality and safety of our chemical and pharmaceutical products, no one would be interested in purchasing...

What Is Radiolabeling, And Why Does It Matter?

Chemical manufacturing, particularly when it comes to drug research and pharmaceuticals, is one of the larger industries within the United States. However, most people across the country don't fully understand many of the basic principles of this field, despite how often they're used by chemical manufacturers for scientific research and study. Radiolabeling, for example, remains...

3 Reasons Cleanrooms Are Important in Manufacturing

Did you know that a fume hood in a laboratory has to be checked at a minimum once a year by a certifier that is independent to ensure that it has the correct airflow that meets CAL/OSHA standards? Whether it’s in a GMP API manufacturing lab or chemical manufacturers, these standards have to be met...

From Purity to Storage: How to Properly Handle Chemicals

Chemical substances go through a long process before commercial use, and it's essential that all steps are followed in order to meet GMP standards. From checking for chemical purity, handling substances, and maintaining a cleanroom, chemical handlers, such as pharmacies, should oblige to all set standards.

Clean Rooms For Dirty Environments

Pharmaceutical clean room standards meet good manufacturing practice (GMP) requirements. Clean room standards do not apply to non-sterilized items; however, for sterilized products, clean rooms are required. Even non-"clean" rooms are well ventilated and filtered. And, monitoring and maintaining a pharmaceutical clean room’s humidity--measuring plus or minus 1%--is standard when using state-of-the-art electronic sensing devices....

Chemical Purity: Why Testing Matters

When it comes to testing the purity of chemicals for various applications in the medical and pharmaceutical community, the right testing matters. You want to be compliant with all laws and regulations of the company, whether your company is mostly into the lab work of most projects or you're involved in the final completion of...

How Important Is Chemical Purity In The Pharmaceutical Industry?

Over the years, the pharmaceutical industry has grown in leaps and bounds. Today, they have been able to formulate high-quality drugs to eradicate some of the deadliest diseases in the world and control the rest. The acceptability and efficacy of these drugs is reliant on the purity of the chemical substances used for medicinal effect...

Top 5 Methods of Assessing Chemical Purity

The United States stands as the largest chemical producer in the world. However, the accolades should be directed to the chemical manufacturers who are involved in mixing these chemicals and coming out with a particular chemical that is used for a particular role. These manufacturers are always involved in a hard and complex task of...

Types of Radiolabeling

Isotopic Labeling Radiocarbon dating, the backbone of Isotopic Labeling, was developed by physicist Willard F. Libby in the 1940s. Over the last 80 years, there have been a number of advances that have increased the scope and application of Libby's method. This is mostly done with radiolabeling.

Ductless Fume Hoods: 5 Benefits That Every Clean Room Can Take Advantage Of

The U.S. holds over 45% of the global pharmaceutical market. Our dominance of scientific and medical fields has allowed us to raise the bar when it comes to the development and circulation of life-saving and life-changing medications. Before these medicines can be offered to the general public, however, they must undergo a grueling testing period;...

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