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Serial No. A. D (Revenue)/20 Dated: Drug Regulatory Authority of Pakistan Ministry of NHS Islamabad****To: Subject: VERIFICATION OF SERVICE FEE CHAPLAINS DEPOSITED IN ALLIED BANK UNDER THE DRAW ACCOUNT
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The drug regulatory authority is a government agency responsible for ensuring the safety, efficacy, and quality of drugs and pharmaceuticals. It oversees the approval of new medications, monitoring of existing drugs, and enforcement of regulations.
Pharmaceutical companies, manufacturers, distributors, and individuals involved in the development and distribution of drugs are required to file with the drug regulatory authority.
To fill out a filing with the drug regulatory authority, you must complete the designated forms, provide required documentation, and submit any necessary fees as outlined by the authority's guidelines.
The purpose of the drug regulatory authority is to protect public health by regulating drugs and ensuring that they are safe, effective, and produced in accordance with established standards.
Information that must be reported includes drug formulation, manufacturing processes, clinical trial data, safety information, labeling details, and any adverse event reports.
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