Chemistry, Manufacturing, and Controls (CMC) services

The CMC Services category covers in-depth scientific and regulatory insights on the development, manufacturing, and quality control of pharmaceutical products across the drug development lifecycle. This section explores key aspects of CMC strategy, including drug substance and drug product development, process optimization, analytical method development and validation, stability studies, impurity profiling, and regulatory documentation for IND, NDA, ANDA, and global submissions.

At ResolveMass Laboratories Inc., we share expert perspectives on CMC challenges, regulatory expectations, and best practices to help biotech companies, pharmaceutical manufacturers, and CRO partners accelerate development timelines while ensuring product quality, safety, and compliance. These blogs are designed for scientists, regulatory professionals, and decision-makers seeking technically rigorous, actionable guidance on CMC activities in modern drug development.