Company Profile

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    Tel: 98 (21) 88332272

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  • Tel:98 (21) 88332272
  • Fax:98 (21) 88630677
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  • City:
  • Street:Yusefabad, Jahanara Ave, 23rd St., No 8, Tehran 1438933743 Iran
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    About us

  • Welcome To Our Site!

  • Arasto is the first private sector manufacturer of Active Pharmaceutical Ingredients (API) in Iran. Founded in 1991, Arasto has been supplying APIs to domestic and international clients since 1994. Regulatory Affairs, Sales and Marketing and other administrative functions are conducted through our head office in Tehran. Research and Development, Manufacturing and QA/QC Departments are located in Kaveh Industrial Park, 90 km south of Tehran.

    FACILITIES
    ? 21,000 sq meter complex includes R&D and QC laboratories, pilot, production and packaging, utilities, water treatment, tank farm and raw material and API warehouses
    ? Total glass-lined and stainless steel reactor volume of 65,000 liters. Reactor volumes range from 250 to 5000 liters.
    ? Extensive water treatment facilities
    ? Consistently lower levels of BOD and COD of effluent water than those required by the Environmental Protection Organization

    RESEARCH AND DEVELOPMENT
    ? Comprised of a core of Ph.D. and M.Sc. chemists and Pharm.Ds with supporting technical staff
    ? Close scientific ties with a number of major academic institutions
    ? Inventorship of over 300 US and international process and product patents to our scientists
    ? Development of non-infringing process patents based on client specifications

    QUALITY CONTROL AND QUALITY ASSURANCE
    ? State-of-the-art equipment such as HPLCs, GCs, UV, IR Atomic Absorption, etc.
    ? Access to high-end analytical instruments such as high resolution 1H and 13C NMR, Mass Spec, X-ray and Powder X-ray through academic institutions
    ? Continuing in-house and off-site training of personnel on quality-related issues

    CURRENT GOOD MANUFACTURING PRACTICE
    ? Strict adherence to over 2000 comprehensive Standard Operating Procedures (SOPs)
    ? Strict adherence to cGMP guidelines as set by FDA and ICH
    ? Continuing in-house and off-site training of personnel on cGMP issues

    REGULATORY AFFAIRS
    ? Plant Master File (Type I) and Drug Mater File (Type II) on all products
    ? Submission of the open portion of DMFs to clients for Regulatory Affairs
    ? DMFs registered in Europe and Canada

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