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Corporate
Corporate Profile 2025
Company overview — history, capabilities, facilities, leadership, and global reach. For partners and regulators.
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Corporate
PDF
Laborate Pharmaceuticals — Corporate Profile 2025
Company overview — history, manufacturing capabilities, international reach, therapeutic focus areas, milestones, and leadership. For partners and regulators.
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Certification
PDF
WHO-GMP Certificate — Panipat Formulation Facility (Unit I & II)
Current WHO-GMP certificate covering oral solid dosage forms, liquid orals, topical preparations, and ophthalmic products. Valid 2024–2027.
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Catalogue
PDF
Laborate Master Product Catalogue — 1,500+ Formulations
All formulations across every therapeutic category, division, dosage form, pack size, and regulatory status. Updated Q1 2025. For partner evaluation and dossier preparation.
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Corporate
PDF
Annual Report FY 2024–25 — Financial & Operational Performance
Audited financial statements, manufacturing metrics, export revenue, R&D investment, sustainability commitments, and strategic outlook for FY ended 31 March 2025.
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Corporate
Annual Report FY 2024–25
Audited financials, manufacturing performance, export breakdown, R&D investment, and strategic outlook for FY ending March 2025.
PDF
Certification
WHO-GMP Certificate — Panipat Unit I
Current WHO-GMP certificate for oral solid dosage forms, liquid orals, and topical preparations. Valid 2024–2027.
PDF
Catalogue
Master Product Catalogue 2025
All 1,500+ Laborate formulations — therapeutic categories, dosage forms, pack sizes, regulatory status, and division assignment. Updated Q1 2025.
PDF
Certification
ISO 9001:2015 Certificate — Quality Management System
ISO 9001:2015 QMS certification covering all five Laborate facilities. Issued by Bureau Veritas. Scope: pharmaceutical manufacturing and R&D.
ZIP
Brand
Brand Identity Guidelines & Asset Pack 2025
Official logo files (SVG, PNG, EPS), colour palette, typography guide, brand voice, and approved photography. For media and partner use only.
XLSX
Export
Export Product List — UAE & GCC Markets
Full product list registered and available for export to UAE and GCC — generic names, pack sizes, shelf life, registration status, and pricing reference codes.
PDF
Technical
CDMO Capabilities Whitepaper — Contract Development & Manufacturing
Technical deep-dive into Laborate's CDMO offering — formulation development, scale-up, analytical method development, process validation, and regulatory filing support.
PDF
Manufacturing
Facility Brochure — Paonta Sahib Formulation Plant
Overview of the Paonta Sahib facility — installed capacity, dosage forms, equipment, quality infrastructure, environmental management, and key regulatory approvals.
PDF
Scientific
Bioequivalence Study Summary — Amoxicillin 500 mg Capsules
Published bioequivalence data — pharmacokinetic parameters, statistical analysis, ISCR classification, and WHO prequalification cross-reference for Amoxicillin 500 mg.
PDF
Regulatory
DCGI Manufacturing Licence — Atorvastatin 10 mg Tablets
Drugs Controller General of India manufacturing licence and product approval for Atorvastatin 10 mg film-coated tablets. Issued under Drugs and Cosmetics Act 1940.
PDF
Catalogue
Elite Division Product Catalogue — Branded Generics Portfolio
The complete Elite Division branded generics range — cardiovascular, anti-infective, gastroenterology, respiratory, and neurology portfolios with full pack size listings.
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