- Regulatory Affairs
As one of the most emerging pharmaceutical player in the export market, we are at the forefront in manufacturing general therapeutic and antibiotic drugs. We have gained a meaningful presence in the domestic market in the early 2016 with more focus on therapeutic segments like Orthopedic, Gynecology, Gastro and General segments.
We have an active presence in Gujarat, Maharashtra, Karnataka, Madhya Pradesh, Chattisgarh and have a vision to expand to the other territories like Uttar Pradesh, Bihar and Rajasthan.
We deliver products, technologies and services to help meet the needs of our customers. With a strong team of highly qualified Sales and Marketing professionals, our vision is to provide quality medicines at affordable prices.
Ratnamani Healthcare provides solid oral dosage product development, scale-up and manufacturing services to the global pharmaceutical market.
With over 6 years in the service business, we have proven expertise in solid oral drug product development, process design/process improvement, tech transfer and commercial scale cGMP manufacturing.
All the services we offer to our partners are provided with the greatest attention to quality and customer service. Our manufacturing business is driven by excellence in what we do’, which through our Operational Excellence program, gives you the reassurance that your product will be guided through our facilities to exacting specifications.
Experience and Approvals
- 4+ year history in business with proven track record and having following approvals,
- ISO 9001 : 2008
- NAFDAC- NIGERIA
- DPM- IVORY COAST
- PPB - KENYA
- CD & DA SRILANKA
- FOB - GHANA
- MOH - LIBIYA
The industry trusts us
- 10+ leading pharma companies are partners of ours
Ratnamani Healthcare is also having presence in several countries,
- Burkina Faso
- Ivory Coast
- Sierra Leone
- Dominican Republic
We have a competent regulatory department with qualified & experienced personnel who prepare dossiers in ACTD /CTD formats as per the guidelines of Ministry Of Health of different countries.
Dossiers are prepared as per requirred regulations which complies to highest regulatory standards.
The regulatory affair department at RHC keeps the track of ever-changing scenario and regulations in the pharmaceutical world. Number of dossiers has been submitted in different countries.
|ASIA-PACIFIC||Myanmar, Philippines, Cambodia, Sri Lanka, Thailand, Vietnam, Nepal, Mongolia|
|AFRICAN ZONE||Kenya, Zambia, Botswana, Burundi, Angola, Rwanda, Ghana Mozambique, Sudan, Francophone Region, Somalia, Libya, Nigeria, Guinea Conakry|
|CIS ZONE||Romania, Uzbekistan, Kyrgyzstan, Georgia, Turkmenistan, Tajikistan, Azerbaijan|
|LATIN AMERICA||Ecuador, Costa Rica, Guatemala, Dominican Republic, Nicaragua, Bolivia, Peru, Cuba, Trinidad, Tabago|
New Submission in 2017