UNIPHARMA PHARMACEUTICAL GUIDLINE
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Universal Pharmaceutical Industries "UNIPHARMA" is one of the prominent advanced firms that is specialized in Pharmaceutical Industries, UNIPHARMA was a Limited family company established in 1990, Construction was performed in compliance with GMP standards set by WHO and per cooperation with experts from the best international pharmaceutical firms, for which UNIPHARMA was manufacturing their products under license and under direct supervision of them to affirm quality control and quality assurance. UNIPHARMA then became a Company a Limited Legibility starting from the year 2012 .
UNIPHARMA now achieves manufacturing pharmaceutical products according to most current GMP rules and high pharmaceutical standards .UNIPHARMA has been recently acquired the Plant registration and got:
- GMP from Russian Federation MOH.
- National Medicinal board at Sudan MOH.
- The up-to-date 3 ISO's certifications :
- Quality Management ISO 9001/2015
- Environmental Management ISO 14001/2015
- Occupational Health & safety Management ISO 45001/2018
being awarded from the German Company Royal Cert .
UNIPHARMA operates by balanced system among administration, production, marketing and promotion by applying electronic communication systems and computer programs in most of its activities and trying to develop such systems constantly.
UNIPHARMA products cover most of treatment fields such as:
- Cardio-vascular medicines
- Respiratory Tract medicines
- Central Nervous System medicines
- Dermatological medicines
- Gastrointestinal medicines
- Metabolism Disturbance medicines
- Anti-biotics medicines
- Antiseptics, etc.
The present production lines at UNIPHARMA are:
- Film coated tablets as IR or ER
- Plain Tabs
- Sugar Coated Tabs & Slow Absorbed Tabs.
- Effervescent Tabs.
- Capsules as IR and ER
- Syrups , Drops & Suspensions
- Dermatological "Creams, Ointments and Gels
- Dental paste.
- Medical shampoos
- Disinfectant solution
Marketing and Exportation:
UNIPHARMA, our firm, and since its establishment has paid special attention for export, noting that this care has continuously increased owing to the constant demand of the foreign markets for our products, which are distinguished by their high quality and assured by complying with MOH , GMP and GLP requirements and Standards.
Also, our previously manufacture under license from many well-known International Pharmaceutical Firms and their valuable contribution by supplying us with the technical assistance and guidance as well as Know How, all of which gave us the basic support to manufacture the most renowned products of our Licensors. (Please revert to the lists of our Licensors and our products.)
To ensure the satisfaction of our agents, our export department takes care of the various aspects of the process such as scientific activities of marketing, sales and training, as well as supplying our team with the various scientific studies and required documents for the health registration and export of our products per the requirements and conditions of each country.
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