North Biotech works with various governments, health ministries, agencies and NGOs.
Our products are distributed in more than 20 countries.

The main responsibility of all government drug regulatory agencies across the globe is to ensure that all products made available to its citizens conform to acceptable standards of quality, safety, and efficacy.

Our highly experienced registration department deals with all matters relating to the registration of our products according to the GMP regulations of different countries.

FACILITY INSPECTION
We realize that the future of our company depends on our continued product improvement and market expansion. Facility inspections are a top priority for us and their results reflect our policy of constant improvement and meticulous attention to detail.
In order to help our factories to be GMP approved by different countries, we try to host government inspectors from abroad to make the pre-audit when preparing to enter new markets.

DOCUMENTATION
Proper documentation is essential in almost every aspect of the pharmaceutical industry. Whether for product registration, factory inspection, or internal quality control, our regulation affairs department work hard together with our partners all the time.

We are highly specialized in the export process and have vast experience with documentation for product registration. Till now we have good experience to prepare both CTD and ACTD dossiers according to the requirements of different countries.
OUR SUCCESSFUL REGISTRATION