WHO-GMP Certified API & Pharmaceutical Intermediate Manufacturing Facility
Four Decades of Pharmaceutical Manufacturing Expertise
Globally Recognized Quality & Regulatory Compliance for API Manufacturing
We are WHO-GMP Certified and have Written Confirmation (WC) for export to Europe.
With regulatory approvals from Japan PMDA and European authorities.
API are manufactured as per ICH guidelines, WHO- GMP and ISO certified processes.
Our Quality Control is 21CFR Part 11 compliant.
Facility for Speciality Chemicals & Intermediates
Advanced chemical intermediates and specialty compounds designed for pharmaceutical synthesis and research applications.
Our portfolio includes complex organic molecules with precise specifications, supporting innovation in drug development and manufacturing processes worldwide.
Created dedicated facilities for specific reactions like Nitration, Oxidation, Sulfonation and Chloro - Sulfonation.
Our key to success is in synthesis of Backward and Forward integration with process optimization and improvisation.
We are a leading global provider of intermediated and speciality chemicals like Sulphonyl Chlorides, Amides, Acids and its derivates.
Trusted by Global Pharmaceutical Leaders
Production Capacity
3 streams of production line with WHOGMP Certification
Audited Excellence
Regularly audited by top Indian and international firms
Client Growth
Exclusive supplier to Teva, Sanofi, Bayer & Lonza for 15–20 years