Our knowledge and comprehension of the market demands and our facilitated field testing allows us to adapt to the rapidly changing demands of the market and gives us the flexibility to introduce our products into new markets. The general philosophy of ARVET hinges upon the fact that drug quality is an accumulative characteristic that originates from the prior stages of drug processing and can not be substituted by the final quality assessment. Consequently, our factory was established to comply with the requirements of Good Manufacturing Practices (GMP) and standards set forth by the Food and Drug Administration (FDA). All stages of production, packaging and storage are subject to direct and indirect monitoring through a comprehensive quality assurance system that complies with the ISO 9001: 2015 standard. As a result of its full understanding of business and public commitments, ARVET has adopted precautionary measures for environmental protection. A comprehensive environmental management system corresponding to the ISO 14001: 2015 requirements has been adopted to demonstrate a sound overall environmental performance & OHSAS 18001:2007 .
We highly believe that meeting the market demands and efficient control over the raw material, semi-finished, and finished products are key factors determining success in penetrating new markets. Therefore, ARVET has equipped itself with state-of-the-art laboratories that consist of:
1- Research and Development Lab: Drug formulas are proposed according to the market demands and field studies carried out by our experts. The R&D Lab delivers the required drug stability testing according to the information received by those experts.
2- Quality Control Lab: This laboratory delivers all required testing to ensure conformity of raw, intermediate, finished, and packaging materials to the set standards. Specifically, finished products are subject to testing according to the standards set by BP and USP.
3- Microbiology Lab: Product assay is a key determinate of product conformity. This lab focuses on testing product biological assay (potency) in both concentrated and diluted forms as well as ensuring that products are free from bacterial or fungal contaminants.