Regulatory clarity
for India’s life-science market.
Rihim Pharma Consultancy works as your own regulatory affairs department: pharma, medical devices, cosmetics and food products, from strategy to licence.
- 8500+
- Regulatory submissions
- 500+
- Clients served
- 100%
- Successful approvals
- 20+
- Years of experience
01
Areas of service
One partner for every Indian regulatory approval, with CDSCO, DCGI and FSSAI.
- 01Medical Devices & IVDEnd-to-end licences for importers and manufacturers of medical devices and diagnostic kits.MD-14 · MD-5 · MD-26
- 02Pharma (DCGI)New drug approvals, FDC approvals, import and registration, and manufacturing approvals.New Drugs · FDC · Import
- 03Clinical TrialsGlobal clinical trial and BA/BE NOCs, and ethics committee registration.CT NOC · BA/BE NOC · Ethics Committee
- 04Vaccines & BiotechRegulatory pathways for vaccines and biotech products entering the Indian market.Vaccines · Biologicals
- 05CosmeticsImport registration and manufacturing approvals for cosmetic products.Import Registration · Mfg. Approvals
- 06Food & NutraceuticalsFSSAI approvals for nutraceuticals and food supplements.FSSAI · Nutraceuticals
02
Why Rihim
An extension of your regulatory team.
A regulatory company that never ignores the science behind your product.Rihim’s approach
- 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.
Regulators we work with
- CDSCO
- DCGI
- FSSAI
- BIS
- ICMR
- Legal Metrology
- WPC
Let’s plan your next approval.
Talk to a regulatory expert518-519, Ring Road Mall, Rohini Sector-3, New Delhi 110085 · info@rihimpharma.com · +91-11-47564040