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Drug Regulatory Authority of Pakistan
The Drug Regulatory Authority of Pakistan is responsible for providing effective coordination and enforcement of the Drugs Act to regulate therapeutic goods. It ensures that medical and pharmaceutical products meet prescribed standards of safety, quality, and efficacy for citizens.
ڈرگ ریگولیٹری اتھارٹی آف پاکستان علاج کی مصنوعات کو منظم کرنے کے لیے ڈرگز ایکٹ کی موثر کوآرڈینیشن اور نفاذ فراہم کرنے کی ذمہ دار ہے۔ یہ اس بات کو یقینی بناتی ہے کہ طبی اور فارماسیوٹیکل مصنوعات شہریوں کے لیے حفاظت، معیار اور افادیت کے مقرر کردہ معیار پر پورا اترتی ہیں۔
What it offers
- What We DoOverview of regulatory functions including registration, licensing, and market surveillance of therapeutic goods.
- Organizational StructureInformation on the institutional hierarchy and functional chart of the regulatory authority.
- Executive ManagementDirectory of executive management personnel and division directors.
- Legislative ActsAccess to legal acts and statutory regulatory orders governing therapeutic goods.
- Central Licensing BoardDetails regarding the licensing board members and establishment oversight.
- Quality PolicyQuality management objectives and policies ensuring adherence to international standards.
- Pharmaceutical DrugsInformation and guidelines regarding pharmaceutical drugs for human or veterinary use.
Independent summary, drafted from dra.gov.pk on 2026-10-02. Not affiliated with Drug Regulatory Authority of Pakistan; the official website is the authority.
