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 a mystery to many people outside of the industry. So how does radiolabeling work? What are radiolabeled compounds used for?
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 in every lab and cleanroom.
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.
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. Let’s look at the specifications of a clean room.
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 products and medical services, chemicals in the air can pose a safety risk and hazard. You can also be in health violation if chemical purity is not up to par.
Laboratories often replace their fume hoods for one main purpose: old age. The replacement process is something that is a concern of around 20% of laboratory owners and a third of the fume hoods replaced are old and outdated. You don’t want to put your lab technicians or other professionals at risk of injury or inhaling potentially harmful fumes, so you should consider assessing chemical purity in your establishment. Here are reasons why this matters, even if you feel like you are already abiding by all guidelines.
Your Labs May Not Be As Safe As You Think
While you have never had any quality control issues before when you do your regular routine of assessing chemical purity, you still don’t know if you are up to code with everything. GMP quality assurance is essential to operating a safe and legal laboratory so you should have the chemicals tested and have air quality assessed on the regular. This can be done in accordance with the recommendations of your quality specialist, or you can do this measure as recommended by your local state laws.
Your Labs Get Fully Tested for Quality
The best way to ensure the safety of your establishment is to have records that you work hard to keep your laboratory updated and sound. When you work with a variety of different chemical manufacturers and want to make sure you aren’t imposing on chemical purity in any way, you can help make your establishment more attractive for research and testing purposes. Universities, independent pharmacies, and other establishments may see your company in a better light and extend their service needs to your lab over others in your community.
However you want to improve the safety of your laboratory, you can do so by having your chemical purity tests done on the regular. Your specialist will be able to give you what you need for accurately assessing chemical purity in your office, labs, pharmaceutical sectors, and more.
