Incoming Material
Each API and excipient is sampled and tested against its specification. Nothing enters production without an approved analysis.
Quality & Compliance
Quality that speaks for itself
We take pride in the quality of our medicines. A GMP certification by the World Health Organization is a testament to our commitment to producing high-quality, safe and effective pharmaceutical products that meet global standards.
Our Framework
Four gates every batch must pass before it reaches a patient
Compliance with stringent guidelines is how we ensure our customers receive products that are safe and effective for their intended use — not a checklist we complete after the fact.
In-Process Control
Defined hold points capture weight variation, hardness, friability, disintegration and assay during the run.
Environment Control
Temperature, relative humidity and differential pressure are monitored across manufacturing and storage zones.
Batch Release
The complete batch record and analytical results are reviewed and signed off before dispatch.
Quality Management System
Continuous review. Constant upgradation.
Our products testify to prioritising consumer health by adhering to the highest industry standards. We operate a Quality Management System for every batch and ensure continuous review and constant upgradation of process and product.
- Documented SOPs covering production, packing, storage and dispatch.
- Deviation and complaint handling with root-cause analysis and CAPA.
- Stability studies to support shelf-life claims through the product lifecycle.
- Periodic vendor qualification and audit of raw-material suppliers.
Analytical QC laboratoryCommon Questions
Quality, answered plainly
If your question is not here, our quality desk will answer it directly.
Are your products manufactured in a WHO-GMP certified facility?
Yes. Our manufacturing partners operate under a WHO-GMP framework, and our product licences are issued against those facilities. Documentation is shared with trade partners on request.
How do you handle a product complaint or adverse event?
Every complaint is logged, investigated and closed with a documented root-cause analysis and corrective action. Adverse events are reported to the appropriate authority within statutory timelines.
Can I get a Certificate of Analysis for a specific batch?
Yes — batch-specific COAs are available to distributors and institutional buyers. Share the batch number and pack configuration with our team and we will provide the corresponding certificate.
Do you support third-party or private-label manufacturing?
We do. We develop and manufacture third-party and private-label formulations for partners across India and export markets, including packaging and documentation support.