The CDMO Division of Arbro Group
Arbro's CDMO vertical, operated through Arbro Formulations, delivers integrated, compliant, globally market-ready products — providing end-to-end contract development and manufacturing services across pharmaceuticals, cosmetics, and nutraceuticals.
Our USFDA-inspected, WHO-GMP-certified, and NABL-accredited facilities span Delhi, Haryana, Himachal Pradesh, and Karnataka. We specialize in transforming ideas into finished products — from formulation development and prototype creation through safety studies, claim substantiation, and full-scale manufacturing.
With a special focus on emerging brands and lower middle-market companies, we offer quality manufacturing partnerships without enterprise-level minimums.
Focus Areas
Formulation Innovation
Cutting-edge R&D capabilities to transform ideas into market-ready formulations across pharmaceuticals, cosmetics, and nutraceuticals.
Scalable Manufacturing
USFDA-inspected, WHO-GMP-certified facilities across Delhi, Haryana, Himachal Pradesh, and Karnataka — ready for pilot to commercial-scale production.
Regulatory Excellence
End-to-end regulatory support ensuring every product meets domestic and international compliance standards for seamless market entry.
Core Offering
Idea to Formulation
Comprehensive formulation development that takes your product concept through research, prototyping, and optimization to a market-ready formulation.
Prototype Development
Rapid prototype creation with iterative refinement, enabling efficient product development cycles and faster time-to-market.
Safety Studies & Claim Substantiation
Rigorous safety evaluation and scientific claim substantiation studies to validate product efficacy and support marketing claims.
Contract Manufacturing
Full-scale GMP-certified contract manufacturing services delivering consistent quality, regulatory compliance, and scalable production capacity.
Packaging & Labeling
Complete packaging design, development, and labeling services compliant with domestic and international regulatory requirements.
Regulatory Filing & Market Entry
End-to-end regulatory dossier preparation and filing support for CDSCO, USFDA, EU, and other global markets.
Product Categories
Pharmaceuticals
Tablets, capsules, syrups, injectables, ointments, and topical formulations under WHO-GMP standards.
- Tablets & Capsules
- Liquid Orals & Syrups
- Topical & Dermal
- Injectables
Cosmetics & Personal Care
Skincare, haircare, and personal care products under ISO 22716 and GMP-certified manufacturing.
- Serums & Creams
- Shampoos & Conditioners
- Sunscreens & Lotions
- Face Masks & Packs
Nutraceuticals
Health supplements, functional foods, and herbal products with full safety and efficacy validation.
- Capsules & Tablets
- Powders & Sachets
- Gummies & Soft Gels
- Herbal Formulations
Manufacturing Infrastructure
State-of-the-art, multi-location manufacturing infrastructure designed for flexibility, quality, and scale.
Why Choose Arbro CDMO
End-to-End Under One Roof
R&D, formulation, manufacturing, testing, clinical research, training, and certification — all integrated capabilities under one organization.
12,000+ Global Clients
A proven track record serving over 12,000 clients worldwide across the pharmaceutical, cosmetic, and nutraceutical sectors.
Multi-Facility Network
USFDA-inspected, WHO-GMP-certified, and NABL-accredited facilities strategically located across four Indian states.
Our CDMO Process
Discovery & Consultation
We understand your product vision, target market, regulatory requirements, and manufacturing needs.
Formulation & R&D
Our R&D team develops and optimizes the formulation, creates prototypes, and conducts feasibility studies.
Testing & Validation
Comprehensive stability, safety, and efficacy testing with claim substantiation and regulatory documentation.
Scale-Up & Manufacturing
Pilot batch to commercial-scale production with full quality assurance and packaging support.
Accreditations & Certifications
Our manufacturing facilities operate under the highest quality standards — USFDA-inspected, WHO-GMP-certified, NABL-accredited, and ISO-compliant — ensuring every product meets international benchmarks for safety and quality.
Request a Manufacturing Quote
Share your product requirements and our CDMO team will get back to you within 24 hours with a detailed proposal.
Looking for a Manufacturing Partner?
End-to-end R&D, formulation, manufacturing, testing, clinical research, training, and certification — all under one roof.
Get a Quote