5 GMP-certified manufacturing facilities across India. 40+ years of pharmaceutical excellence. Delivering to 40+ countries.
Laborate operates a vertically integrated pharmaceutical manufacturing network — from API sourcing through formulation, packaging and distribution. Every facility is independently certified, quality-audited and production-optimised.
"We do not merely manufacture medicines.
We engineer the trust that reaches every patient."
At Laborate, manufacturing is not a function — it is the foundation. Every gram of raw material, every production run, every quality test is executed against a singular standard: the medicines leaving our facilities must work exactly as intended, every time, for every patient.
From a single plant in Panipat to a network of five GMP-certified facilities — a story of consistent growth, quality and global reach.
Laborate Pharmaceuticals established in Panipat, Haryana. First manufacturing facility inaugurated with solid oral dosage form production.
FoundingFirst WHO GMP certification awarded. Laborate begins supplying international markets across Africa and Southeast Asia.
RegulatoryPaonta Sahib Sterile & Export Plant commissioned. Sterile injectables and ophthalmic manufacturing capacity added.
ExpansionPanipat Unit I receives USFDA approval — marking Laborate's entry into the US-regulated pharmaceutical export market.
RegulatoryProduct portfolio crosses 1,000 formulations across therapeutic categories. Annual unit production exceeds 1 billion.
ScaleEU GMP certification achieved across sterile manufacturing operations — establishing Laborate as a preferred European-market supplier.
RegulatoryKundli manufacturing facility inaugurated in Haryana — fifth GMP-certified plant, strengthening northern India's pharmaceutical corridor.
ExpansionFull compliance with India's revised Schedule M (upgraded GMP norms) across all 5 facilities — setting the standard for domestic pharmaceutical manufacturing.
ComplianceAcross our 5 facilities, Laborate produces 8 major dosage form categories — from solid oral formulations to sterile injectables and ophthalmic preparations.
End-to-end pharmaceutical manufacturing capabilities — from sterile and non-sterile formulation through specialist segments to export-grade regulatory compliance.
Class A/B cleanroom production of injectables, ophthalmic solutions and sterile suspensions under ISO 5 classified environments.
High-volume oral solid dosage manufacturing — tablets, capsules, dry syrups and liquid formulations across multiple production lines.
Dedicated, segregated Beta Lactam manufacturing facility with independent air handling, materials flow and cross-contamination controls.
Fully segregated cephalosporin manufacturing block with dedicated equipment, personnel gowning and environmental monitoring protocols.
In-house NABL-accredited quality control laboratories at every facility — chemical, microbiological and physical testing from raw material to release.
Automated blister packaging, strip packaging, bottle filling and cartonating lines — configured for both domestic and export market specifications.
Export-grade production lines calibrated to destination-market regulatory requirements — USFDA, EU, ANVISA, TGA, WHO Prequalification.
Integrated regulatory affairs team managing CTD dossier preparation, DMF filings, inspection readiness and ongoing post-approval changes across 40+ markets.
Formal technology transfer capabilities — process scale-up, analytical method validation and site-to-site product transfers for CDMO partners.
Every Laborate manufacturing facility operates to the highest international pharmaceutical standards — independently verified and continuously maintained.
Strategically located in Haryana and Himachal Pradesh — India's pharmaceutical manufacturing corridor — Laborate's five WHO-GMP certified plants cover every major dosage form category.
5 strategically located facilities across North India — each independently certified and specialised for different dosage forms and market requirements.
PLT-01
Panipat, Haryana
PLT-02
Paonta Sahib, Himachal Pradesh
PLT-03
Karnal, Haryana
Laborate's CDMO division offers contract development and manufacturing services for global pharmaceutical companies. From formulation development and process scale-up to full-scale GMP manufacturing and regulatory support — we are your end-to-end manufacturing partner.
GMP Certified Facilities Available for CDMO
Dosage Form Capabilities
Export Markets Covered by Regulatory Team
Discuss CDMO services, contract manufacturing or facility audits with our specialists.
