A 12,000 sq. ft. R&D-backed facility in Rohtak, built to WHO, US FDA and EU GMP norms across six dosage forms.
Our state-of-the-art manufacturing plant and 12,000 sq. ft. R&D laboratory are located in Rohtak, Haryana — just 70 km from New Delhi and well connected to international logistics hubs. Every line is designed to international GMP standards with controlled environments, validated processes and full batch traceability.
Coated and uncoated oral solid dosage forms.
Hard-gelatin capsule formulations.
Oral liquid syrups and suspensions.
Semi-solid topical preparations.
Oral and external liquid preparations.
Sterile lyophilised injectable powders.
From raw-material qualification to final batch release, every step is documented and verified.
Incoming materials are sampled, tested and qualified against specification before release to production.
Critical parameters are monitored at every production stage in controlled environments.
Each batch undergoes full analytical, microbiological and stability testing.
Documented review and certificate of analysis before dispatch with full traceability.
Our manufacturing and quality systems are aligned to the norms that international buyers require — supporting product registration across regulated and emerging markets.
Certification marks shown reflect the standards our facility is built and operated to. Documentation is available to qualified partners on request.
We welcome technical discussions and documentation reviews with serious distribution partners.