In pharmaceuticals, every step matters. Right from sourcing raw materials to the final delivery of the end products. Hence, complete traceability is not just a regulatory checkbox, it’s a cornerstone of patient safety to the product's integrity.

At Coral Drugs, we ensure that every batch is fully accounted for & traceable. We maintain end-to-end batch records, raw material traceability, final delivery audit trails as well as complete backward integration. These measures ensure reliability, repeatability & quality controls with complete trust, batch after batch.

We take pride in the fact that our facilities are designed to be inspection-ready at all times. With rigorous in-house quality audits, global regulatory filings (US DMF, CEP, and more), stability data and impurity profiling, we meet and exceed the expectations of a cGMP-certified, audit-friendly site. This proactive approach helps Coral secure faster approvals and build stronger regulatory confidence.

Choosing Coral Drugs means partnering with a manufacturer that values transparency, accountability, and compliance throughout your product’s lifecycle. We believe that safeguarding the supply chain is directly linked to safeguarding patient health.

It's in our belief that traceability isn’t a feature, it’s a foundation.

Follow Coral Drugs on LinkedIn for insights on pharma compliance, traceability, and API manufacturing excellence.

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