Regulatory approvals for India, without the wait.
Rihim Pharma Consultancy works as your own regulatory affairs department for pharma, medical devices, cosmetics and food products.
- CDSCO
- DCGI
- FSSAI
- BIS
- ICMR
- Legal Metrology
- WPC
Every Indian approval,
one partner.
From the first regulatory strategy to the final licence, a team of certified pharmacists handles the complete process.
Medical Devices & IVD
End-to-end licences for importers and manufacturers of medical devices and diagnostic kits.
Pharma (DCGI)
New drug approvals, FDC approvals, import and registration, and manufacturing approvals.
Clinical Trials
Global clinical trial and BA/BE NOCs, and ethics committee registration.
Vaccines & Biotech
Regulatory pathways for vaccines and biotech products entering the Indian market.
Cosmetics
Import registration and manufacturing approvals for cosmetic products.
Food & Nutraceuticals
FSSAI approvals for nutraceuticals and food supplements.
An extension of your regulatory team.
- 01
Regulatory strategy
A clear plan for every product before the first document is filed.
- 02
Pre-screening of documents
Dossiers are checked in-house so submissions go in right the first time.
- 03
Timeline management
Every approval is tracked against its deadline, with regular updates.
- 04
On-demand services
Extend your own regulatory team only when you need it.
Planning a launch in India?
Share your product and timeline. Our team replies with the regulatory pathway.
Talk to a regulatory expert