Arbro Formulations - CDMO Manufacturing Facility
USFDA Inspected | WHO-GMP Certified

Contract Development & Manufacturing

End-to-end CDMO solutions — from idea to formulation to full-scale manufacturing. Serving 12,000+ clients globally across pharmaceuticals, cosmetics, and nutraceuticals.

A 40-Year Legacy of Trust

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.

CDMO manufacturing facility
Contract manufacturing production line Quality control in CDMO facility
12,000+Clients Served
WHO-GMPCertified
4Manufacturing Locations
USFDAInspected
Our Focus

Focus Areas

01

Formulation Innovation

Cutting-edge R&D capabilities to transform ideas into market-ready formulations across pharmaceuticals, cosmetics, and nutraceuticals.

02

Scalable Manufacturing

USFDA-inspected, WHO-GMP-certified facilities across Delhi, Haryana, Himachal Pradesh, and Karnataka — ready for pilot to commercial-scale production.

03

Regulatory Excellence

End-to-end regulatory support ensuring every product meets domestic and international compliance standards for seamless market entry.

What We Offer

Core Offering

01

Idea to Formulation

Comprehensive formulation development that takes your product concept through research, prototyping, and optimization to a market-ready formulation.

02

Prototype Development

Rapid prototype creation with iterative refinement, enabling efficient product development cycles and faster time-to-market.

03

Safety Studies & Claim Substantiation

Rigorous safety evaluation and scientific claim substantiation studies to validate product efficacy and support marketing claims.

04

Contract Manufacturing

Full-scale GMP-certified contract manufacturing services delivering consistent quality, regulatory compliance, and scalable production capacity.

05

Packaging & Labeling

Complete packaging design, development, and labeling services compliant with domestic and international regulatory requirements.

06

Regulatory Filing & Market Entry

End-to-end regulatory dossier preparation and filing support for CDSCO, USFDA, EU, and other global markets.

What We Manufacture

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
Arbro CDMO manufacturing facility - Baddi, HP
Our Facilities

Manufacturing Infrastructure

State-of-the-art, multi-location manufacturing infrastructure designed for flexibility, quality, and scale.

New Delhi R&D Centre, Formulation Lab, Pilot Plant
Manesar, Haryana Analytical Testing & Quality Control
Baddi, Himachal Pradesh WHO-GMP Manufacturing Plant
Bangalore, Karnataka Analytical Testing Lab
Why Partner With Us

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.

How We Work

Our CDMO Process

1

Discovery & Consultation

We understand your product vision, target market, regulatory requirements, and manufacturing needs.

2

Formulation & R&D

Our R&D team develops and optimizes the formulation, creates prototypes, and conducts feasibility studies.

3

Testing & Validation

Comprehensive stability, safety, and efficacy testing with claim substantiation and regulatory documentation.

4

Scale-Up & Manufacturing

Pilot batch to commercial-scale production with full quality assurance and packaging support.

Quality Assurance

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.

NABL
ISO
GMP
FSSAI
BIS
CDSCO
Get Started

Request a Manufacturing Quote

Share your product requirements and our CDMO team will get back to you within 24 hours with a detailed proposal.

Low MOQ Flexible minimums for emerging brands
End-to-End Service Idea to shelf-ready product
WHO-GMP Certified International quality standards

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