The Value of Growing for Regulatory

The Value of Growing for Regulatory

The Value of Growing for Regulatory

Every new product that hits the market, including new pharmaceuticals, must follow regulatory compliance. Regulatory authorities issue guidelines and rules for development, licensing, manufacturing, marketing, labeling, and more. While strict guidelines may seem like a pain, they are highly crucial to pharmaceuticals’ safety and efficacy and their development process. Improved standard methods, efficiency, and costs are a few of the values of growing for regulatory. 

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Different Types of Impurities in Pharmaceuticals

Different Types of Impurities in Pharmaceuticals

An impurity in pharmaceuticals is classified as any component that is not the entity defined as the drug substance. In addition, for a drug product, any component that is not a formulation ingredient is considered an impurity. There are three different types of impurities in pharmaceuticals that API manufacturing companies must be wary of. Below, we provide a more in-depth look at each of these three types of impurities.

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