Meaning :
In the pharmaceutical industry, “CMC” stands for “Chemistry, Manufacturing, and Controls.” It refers to the section of drug development that focuses on the chemical composition, production processes, and quality control of a pharmaceutical product. CMC ensures that the drug is manufactured consistently, meets regulatory standards, and is safe and effective for use. This part of drug development is critical for regulatory approval.
Synonyms :
Drug formulation
Pharmaceutical development
Manufacturing process
Quality assurance
Product development
Drug production
Chemical formulation
Drug composition
Regulatory compliance
Quality control processes
Antonyms :
Non-regulated manufacturing
Uncontrolled production
Unsafe drug development
Inconsistent formulation
Unapproved process
Irregular manufacturing
Unvalidated testing
Lack of quality control
Non-compliant production
Unverified drug composition
Short Sentence Examples :
“CMC is a critical component of the drug approval process.”
“Pharmaceutical companies must meet CMC requirements to gain regulatory approval.”
“The CMC section of a new drug application covers manufacturing and quality standards.”
“CMC ensures that drugs are consistently produced with the correct chemical composition.”
“A comprehensive CMC submission helps guarantee the drug’s safety and efficacy.”
