Intermediates

  • We offer from our manufacturer principals facility located in India with the SOP driven manufacturing activity carried out strictly as per ICH Q7 cGMP guidelines, and several conventional and modern techniques are used for the isolation, semi-synthesis, and purification of our products. The manufacturing processes have been validated to ensure consistent product quality.

    Facilities have been inspected and approved by Regulatory authorities like US FDA, ANSM, KFDA, TGA, CDSCO, etc. They hold GMP certificates and Written Confirmation for most of our products. They have PMDA accreditation for several products

  • We offer this product from an Indian manufacturer having strong API Processing and manufacturing capabilities.
  • We offer this product from the API manufacturing facility located in India consisting of different volumes of reactors suitable to carry the reactions like Catalytic hydrogenations, Chlorination?s, Nitration?s, Alkylation?s, Oxidations, Reductions, Resolutions(chemical), Couplings, etc. The manufacturing unit has a well-equipped ceanroom facility for finished product drying, milling, packing & storage.

    Quality Control is independent of production and is done in-house at the on-site QC laboratory, including GC & HPLC. Documentations are prepared and upgraded as per GMP guidelines like ICH Q7 and other international regulatory guidelines. Regular Internal Quality Audits and GMP Audits to ensure the continuous maintenance of Change control, Document control, Deviation Handling, Complaint handling, Validation Qualification of Equipment, and total Quality system. The unit has an excellent laboratory to conduct experiments on existing products and other new molecules development.

  • We offer this product from a manufacturer in CHINA mainly engaged in R&D and production of pharmaceutical intermediates. Quality management systems are strictly under the supervision of ISO9001 and ISO14001 system.

  • We are offering the product from our Indian manufacturer's USFDA, Japan PMDA, Korea FDA approved site. Their facility is COFEPRIS inspected for several products. Their R&D facility is recognized by the Department of Scientific and Industrial Research (DSIR, Ministry of Science and Technology, Government of India).
  • We are offering the product from our Indian manufacturer's USFDA, Japan PMDA, Korea FDA approved site. Their facility is COFEPRIS inspected for several products. Their R&D facility is recognized by the Department of Scientific and Industrial Research (DSIR, Ministry of Science and Technology, Government of India).
  • We offer this product from an Indian manufacturer focused on developing and manufacturing of Active Pharmaceutical Ingredients (APIs), Pharma Intermediates, Fine Chemicals and Pyridine Derivatives in a cGMP factory with ISO 9001-2008 and ISO 14000:2004 certification.

  • We offer this product from the API manufacturing facility located in India consisting of different volumes of reactors suitable to carry the reactions like Catalytic hydrogenations, Chlorination?s, Nitration?s, Alkylation?s, Oxidations, Reductions, Resolutions(chemical), Couplings, etc. The manufacturing unit has a well-equipped ceanroom facility for finished product drying, milling, packing & storage.

    Quality Control is independent of production and is done in-house at the on-site QC laboratory, including GC & HPLC. Documentations are prepared and upgraded as per GMP guidelines like ICH Q7 and other international regulatory guidelines. Regular Internal Quality Audits and GMP Audits to ensure the continuous maintenance of Change control, Document control, Deviation Handling, Complaint handling, Validation Qualification of Equipment, and total Quality system. The unit has an excellent laboratory to conduct experiments on existing products and other new molecules development.

  • We offer this product from the manufacturer in India, having the manufacturing facility approved by the local FDA authority and CDSCO. The facilities are WHO GMP and ISO 9001:2015 certified with quality systems complying with ICH-Q7 guidelines.

  • We offer this product from a manufacturer in CHINA mainly engaged in R&D and production of pharmaceutical intermediates. Quality management systems are strictly under the supervision of ISO9001 and ISO14001 system.

  • We offer this product from a manufacturer in CHINA mainly engaged in R&D and production of pharmaceutical intermediates. Quality management systems are strictly under the supervision of ISO9001 and ISO14001 system.

  • We offer you this product from an Indian manufacturer manufacturing chiral or achiral homogeneous precious metal catalysts, chiral ligands, API intermediates, and specialty chemicals for customers Globally. They provide technical assistance in their catalyst, chemistry, or process development projects.

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