Every facility, process and formulation is built around validated, auditable systems that satisfy regulators and partners across 30+ countries.
Independently audited on a rolling schedule across all manufacturing units.
Good Manufacturing Practice certified across all lines
Quality management systems certification
Environmental management certification
Registered manufacturing licenses per jurisdiction
Every batch passes through in-process quality checks during manufacturing, finished-product testing against pharmacopoeial standards, and ongoing stability testing under ICH climatic conditions.
Weight variation, hardness, disintegration and content uniformity checks during production.
Assay, dissolution, microbial limits and impurity profiling against IP/BP/USP standards.
Real-time and accelerated stability testing under ICH Q1A climatic zones.
Purpose-built, dosage-form-segregated production units.
Tablet & capsule production, 8 lines, 2.4M units/day capacity.
Syrups, suspensions and cream/ointment filling lines.
Grade A/B cleanroom suite for lyophilised & liquid injectables.
Our regulatory affairs team can share CoAs, stability data and product dossiers on request.