The regulatory practices of Avenierr Pharma (Pvt) Ltd are blue printed by a team of Qualified Pharmacists. It includes the registration of products, product licensing and resolving post-marketing issues amongst others. All dossiers are assessed on specific guidelines put forward by regulatory institutes prior to submitting them to the National Medicines Regulatory Authority (NMRA).

Regular monitoring of the processes adopted by the warehouse personnel are carried out to verify that the required standards are adhered. The regulatory team is given the responsibility of vigilance and adopts CIOMS guidelines according to several agreements signed by the company with foreign principals of the Avenierr Pharma (Pvt) Ltd.

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