MoH: Ministry of Public Health
MoH website: https://moph.gov.af/en
Regulatory Authority: Afghanistan Food and Drug Authority National Medicine and Health Products Regulatory Authority (NMHRA)
Link for Regulatory Authority: https://afda.gov.af/index.php/en/market-0
In the ever-changing healthcare landscape of Afghanistan, it is critical to effectively regulate medical goods and services. This paper explores the complex pre-marketing processes, including planning and policy, licensing, marketing permits, supply, price, and the vital oversight and management of clinical trials.
The foundation of healthcare regulation is the drafting and revision of legislative documents. Lawmakers in Afghanistan create and amend laws on a regular basis to meet changing needs and conform to global norms. Carefully constructed legislative documents handle licensing, permits, cost, and clinical study regulation.
Beyond the original drug registration procedure, there is a continuous commitment to ensuring the safety, efficacy, and quality of pharmaceuticals.
Cooperation with Stakeholders: Afghan regulatory agencies work closely with pharmaceutical companies, medical practitioners, and other stakeholders to improve post-market surveillance. This cooperative strategy encourages a shared accountability for maintaining pharmaceutical standards, with continual education and communication to address issues and encourage adherence.
Fees: AFN (50,000)
License Validity: 3 years.
Local Authorized Representative: Yes, a local Authorized Representative is required before you place your product on the market.
FSC required: Yes
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Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
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