Drug development is a highly multidisciplinary journey—from target identification and lead compound discovery to clinical trials and market entry. Throughout this process, CMC plays a pivotal role, yet its importance is often underestimated.
In this article, we explore how CMC activities—spanning formulation, manufacturing, and quality control—are essential to ensuring drug candidates are not only effective, but also safe, stable, and reproducible. CMC underpins every stage of development, supporting both regulatory success and product reliability.
Whether you’re in early development or preparing for submission, understanding the value of CMC is key to accelerating timelines and reducing risk.
Read here the FULL ARTICLE.
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