API at Senores

Manufacturing Capabilities API

Senores Group has a decade of experience in manufacturing and developing across a diverse range of therapeutic areas.

Equipped with world-class, technologically advanced manufacturing facilities and systems. We divided our overall facility into different segments, i.e. research and development, manufacturing unit, quality testing, warehousing and packaging unit. All the pharmaceutical formulations are kept safe and pure with the help of all the necessary safety precautions that are followed in the premises set across a large area.

Reaction Type

Manufacturing Capabilities API

Senores has the full-fledged capability to handle a wide range of chemical reactions.

  • Nitration

  • Bromination

  • Friedel-crafts

  • Grignard reaction

  • Hydrogenation

  • Chlorination

  • Esterification

  • Hydrolysis

    Senores has highly advanced and cost-effective manufacturing facilities

    Manufacturing Capabilities API

    • Reactor details – 1.6 KL - 6.3 KL

    • Temperature - -100°C - 200°C

    • Material of construction- SS, GL, SS-GL, MS-GL

    • Compliances – WHO

      Production

      Manufacturing Capabilities API
      • Fully equipped GMP compliant facility
      • Facility designed to manufacture multiple/ bulk quantity products
      • Multi reaction facility
      • Annual capacity: API-120 MT & Intermediates: 480 MT

      Quality Control and Compliance

      Manufacturing Capabilities API
      • Well-equipped testing laboratory
      • Wet lab, instrumentation & Microbiology lab
      • Analysis of raw materials, in-process and intermediates & APIs
      • Stability studies as per global requirements
      • Facility for the storage of retained samples
      • Regular audit of manufacturing facility
      • Standardized waste management and environmental protection system

      Contract development and manufacturing

      Manufacturing Capabilities API
      Senores' comprehensive, GMP contract manufacturing service manufactures bulk pharmaceutical ingredients and intermediates in accordance with the rigorous expectations of global pharmaceutical standards

      Manufacturing services

      • Manufacture API to customer specifications
      • Design and develop manufacturing processes
      • Process optimisation for competitiveness
      • Filing of DMF/CMC for the API
      • Patent protection for processes