Blogs

Proofreading regulated documents in pharma presents unique challenges. Avoid the high risk of costly mistakes with best practices and by leveraging technology.

Medical writing describes a wide range of writing in the fields of medicine and healthcare. Discover more about medical writing and “a day in the life.”

Comparison software offers immense savings, especially in regulated industries. Ask some of the leading pharmaceutical companies. Here are 6 Ways You Save.

We will explore what we mean by readability and what key principles can guide us through regulations to make labeling readable and legible.

The Modernization of Cosmetics Regulation Act of 2022 (MoCRA) is the most significant change to cosmetics regulation since 1938. Are you prepared?

Ten years and $1 billion later, close your eyes and imagine; your product has been approved in the US by the Food and Drug Administration (FDA).

Counterfeit medical products, including drugs and devices, pose a serious global threat to public health.