Why do regulations for controlled substances differ from those for non-controlled medications?

Regulations for controlled substances are indeed more stringent due to the nature of these medications. Controlled substances have the potential for misuse, abuse, and dependency, which necessitates a higher level of oversight to ensure their safe and appropriate use. The stricter accountability measures, including rigorous record-keeping and tracking requirements, are implemented to prevent diversion, monitor prescribing practices, and safeguard public health.

This heightened regulation helps mitigate risks associated with these substances, such as addiction and overdose. In contrast, non-controlled medications do not typically carry the same level of risk and, therefore, do not require the same stringent oversight. This distinction underscores the importance of tailored regulations to address the unique challenges posed by controlled substances in medical practice.