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; clean room standards must be met to ensure that they aren’t tainted or contaminated. From GMP storage conditions to GMP quality control, there are a number of steps and tools that play a major role in this sterile environment. Let’s take a look at some of the benefits that ductless fume hoods in particular offer.

The U.S. is the number one largest national producer of chemical products in the world. Our scientific and medical advancements — and dedication to GMP standards and GMP quality control — allow us to dominate the market; everything from radiolabeled compounds (Tritium, a radioactive isotope of hydrogen, is often used) to GMP synthesis originates in this country. With the new tariffs on Chinese imports, however, that may change.

Storage Conditions and Chemical Purity

Why are storage conditions for drugs so important? How do chemical manufacturers assess purity of chemicals they use for drugs? Why should you care?