Nikan Elixir Bakhtar Pharmaceutical Company was established in 2012 by using new technology and employing specialized and experienced personnel with the aim of producing drugs, and was inaugurated in 2015, Deputy Minister of Research and Technology of the Ministry of Health. Also this production unit is equipped with:
Quality control laboratory
Research and Development Department
80 meters of clean room space
Department of Synthesis Chemistry
Installation and water treatment unit
Collection honors
Our scientific team
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Quality control laboratory
Given that the professional pharmaceutical industry is successful in the world and is in the group of the most powerful industries in the world, it has a great role in improving the quality of human life. Ensuring the maximum safety and efficiency of the products of this industry and as a result guaranteeing the quality of products requires repetitive, sensitive and specific Najzbeh methods and instructions and in accordance with global pharmacopoeias. It has a special priority in the pharmaceutical industry.
Due to the special attention of the company’s management to the quality principle, the quality control laboratory of Nikan Elixir Bakhtar Pharmaceutical Company, with the support of its trained, specialized and experienced personnel and also with modern devices used in analyzing and determining the amount of raw materials and products, the latest quality control instructions. The FDA implements USP, BP, and EP international standards in evaluating the quality of manufactured products as well as in controlling the entire preparation process, from the purchase of raw materials to the warehousing of the final product. This laboratory has 3 personnel, all of whom are specialized and experienced people with academic education and works in various departments of device analysis, microbiology, IPQC, packaging materials control and physicochemical control.
This section has the role of supervising all parts of production (manufacturing and packaging stages). Its purpose is to implement GMP rules in all production processes (from weighing to the final packaging of the product). On the operation of autoclaves, monitoring the observance of GMP principles in all stages of production, monitoring the quality of production equipment, controlling the irrigation system on a daily basis, preparing the necessary SOPs to control raw materials and products in accordance with international pharmaceutical standards and updating and sampling From the final products of
Devices :
Polari meter
pH meter
Conductivity meter
Digital balance
Analytical Balance
High performance liquid chromatography (HPLC)
Digital burette
Oven (25- 250) °C
Water bathes
Dissolution
Magnetic stirrer and rotator
Conductivity meter and Magnetic stirrer
Laboratory Muffle Furnace (200- 1100) °C
Incubators and Ovens
Laboratory centrifuge
Freezer and refrigerator
Autoclaves
Mechanical shake
Disintegration
Ultrasonic – Cleaner
Karl Fischer Titrator
Deionized Water Machine
TLC viewer
Rotary
Furnace
Vacuum Oven