Profile

1) Pharmaceutical Product RegistrationThe Registration Dossier is a comprehensive document that includes all necessary technical data for the approval, registration, or marketing of a pharmaceutical product in a specific country. At Meditrona, we are here to assist you with the registration of your products. Our facility holds accreditations from:

● WHO GMP
● EU GMP
● Other global certifications

We are fully equipped to support you in preparing the required documentation, ensuring compliance with international regulations, and helping you bring your products to market quickly and effectively.


2) Named Patient Supply

Through our Named Patient Programme (NPP), we facilitate access to approved medicines for physicians and patients in cases where these medications are unavailable in their country. Meditrona helps import and supply these medicines, which may be:

● Approved but not yet available for prescription in a specific country
● Approved in one country but not in the patient’s country
● Discontinued in the patient’s country but still accessible elsewhere
● In shortage in the patient’s country

Our dedicated team manages the regulatory and logistical processes, ensuring the safe and effective use of these vital medicines. Physicians can rely on Meditrona to source medications globally and ensure timely delivery to their patients.