Kusum Healthcare
Kusum Healthcare Pvt Ltd. is a young, efficient, and tech-driven pharmaceutical group with a global presence, dedicated to manufacturing high-quality, affordable, and safe medicines. Established in 1997 and headquartered in New Delhi, India, it operates four state-of-the-art manufacturing units in India and Ukraine, all WHO GMP certified and PIC/s compliant. The company has a strong focus on research, development, and regulatory compliance, with a presence in 29 countries across various continents. Its mission is to improve the quality of life worldwide through innovative and reliable pharmaceutical products, emphasizing integrity, responsibility, and excellence.
Industries
Nr. of Employees
small (1-50)
Kusum Healthcare
Kusum Healthcare Pvt Ltd, Department of Pharmacovigilance, D-158A, Okhla Industrial Area, Phase-I, New Delhi 110020, India
Products
Oral solid dosage forms (tablets, chewables, effervescent, ODT)
Finished oral solid formulations for a range of indications and markets.
Topical and semi-solid formulations (creams, gels, ointments, shampoos)
Topical products including creams, gels, ointments and medicated shampoos for dermatology and related indications.
Suppositories, pessaries and enema formulations
Rectal and vaginal dosage forms including suppositories, pessaries and enemas for relevant therapeutic areas.
Granules and powder formulations
Granular and powdered formulations for oral administration and pediatric/OTC formats.
Oral solid dosage forms (tablets, chewables, effervescent, ODT)
Finished oral solid formulations for a range of indications and markets.
Topical and semi-solid formulations (creams, gels, ointments, shampoos)
Topical products including creams, gels, ointments and medicated shampoos for dermatology and related indications.
Suppositories, pessaries and enema formulations
Rectal and vaginal dosage forms including suppositories, pessaries and enemas for relevant therapeutic areas.
Granules and powder formulations
Granular and powdered formulations for oral administration and pediatric/OTC formats.
Services
Collection and processing of adverse event reports and product complaints through dedicated PV channels (toll-free, email, ADR forms); maintenance of pharmacovigilance records.
In-house development of finished-dosage formulations supported by preparation of regulatory dossiers for product registration in CTD and ACTD formats.
Commercial and regulatory support for export markets including local registration facilitation, warehousing and distribution via global offices.
Collection and processing of adverse event reports and product complaints through dedicated PV channels (toll-free, email, ADR forms); maintenance of pharmacovigilance records.
In-house development of finished-dosage formulations supported by preparation of regulatory dossiers for product registration in CTD and ACTD formats.
Commercial and regulatory support for export markets including local registration facilitation, warehousing and distribution via global offices.
Expertise Areas
- Formulation research and development
- GMP pharmaceutical manufacturing
- Regulatory submissions and dossier management (CTD/ACTD)
- Pharmacovigilance and ADR management
Key Technologies
- Automated production equipment for formulation manufacturing
- Finished-dosage form formulation development
- CTD/ACTD regulatory dossier preparation
- GMP-compliant production processes