
Akums Drugs and Pharmaceuticals Ltd.
India's largest CDMO with 15+ facilities, 4,100+ formulations, and WHO-GMP/USFDA/EU-GMP compliance.
India's largest CDMO with 15+ state-of-the-art facilities and 30% domestic market share, manufacturing 4,100+ formulations across tablets, capsules, injectables, APIs, and specialty dosage forms under WHO-GMP, USFDA, EU-GMP, and TGA compliance. Headquartered in Haridwar, India.
Modalities
Development & manufacturing
Structured CDMO capabilities from verified public sources.
Manufacturing (M)
Fill-finish formats
Regulatory clearances
Services
- Formulation Development
- Process Development
- Technology Transfer
- CMC Regulatory Submission Support
- CMC Analytical Development
- Stability Testing & Storage
- Quality Control Testing
- Oral Solid Dosage Manufacturing
- Ophthalmic Manufacturing
- Inhalation & Nasal Dosage Manufacturing
- Topical & Semi-Solid Manufacturing
- Vial Filling
- Lyophilization (Freeze Drying)
- Sterile Fill-Finish & Aseptic Manufacturing
- API Synthesis & Manufacturing
Indications
About this organization
Overview
Akums Drugs and Pharmaceuticals Ltd. is India's largest contract development and manufacturing organization (CDMO) by revenue, production capacity, and clients served. The company operates 15+ state-of-the-art manufacturing facilities and collaborates with 1,500+ pharmaceutical companies to manufacture over 4,100 commercialized formulations.
Core Capabilities
Formulation Manufacturing:
- Tablets and capsules
- Injectable formulations (ampoules, liquid vials, lyophilized vials)
- Soft gels, syrups, and topicals
- Ophthalmic products (preservative-free vials, unit-dose systems, eye drops)
- Nutraceuticals and cosmeceuticals
- Dermatology solutions
- Respiratory solutions (respules, nebulization formulations)
Active Pharmaceutical Ingredients (API): Dedicated API manufacturing capabilities compliant with international regulatory standards, ensuring high-quality raw material supply and supply chain reliability.
Advanced Technologies:
- Form-Fill-Seal (FFS) technology for high-speed sterile manufacturing
- UNIMS® unit-dose delivery system for ophthalmic products
- PRIBSYS™ preservative technology (BKC-free ionic-buffered system)
- Lyophilization for freeze-dried formulations
- Automated aseptic filling systems
Development & Support Services:
- Formulation development
- Technology transfer
- Regulatory support
- Process development
- Quality management systems
Regulatory Compliance
Akums maintains compliance with WHO-GMP, USFDA, EU-GMP, and TGA standards. The company operates an advanced Quality Management System (QMS) and demonstrates a compliance-driven approach across all manufacturing operations.
Market Position
The company holds 30% market share in the domestic CDMO pharmaceutical sector and is recognized as a leader in the Make in India initiative, serving global pharmaceutical and healthcare companies.
Certifications
Locations
Sterile Manufacturing Facility
Haridwar · India
Related companies
Similar profiles by shared services, modalities, and capabilities.
Delpharm- Formulation Development
- Process Development
Bend Bioscience- Formulation Development
- Process Development
Ascendiacdmo- Formulation Development
- Process Development
Lupin Limited- Formulation Development
- Process Development
Grifols Partnership- Formulation Development
- Process Development
Ascendia Pharmaceutical Solutions- Formulation Development
- Process Development
Amneal Pharmaceuticals- Formulation Development
- Process Development
Ardena- Formulation Development
- Process Development
Submit a verified review for this organization.
Markdown mirror: /companies/akums.md