What is the purpose of drug registrations in pharmaceutical regulation?
The purpose of drug registrations in pharmaceutical regulation is to ensure the safety, efficacy, and quality of pharmaceutical products before they are made available to the public. Regulatory agencies require drug manufacturers to submit detailed documentation demonstrating the safety, efficacy, and manufacturing processes of their products. Drug registrations allow regulatory authorities to evaluate and approve drugs for marketing, thereby safeguarding public health and promoting access to safe and effective medications.