Industries We Serve
From pharmaceuticals to food products, we provide end-to-end regulatory support across every major product category in India.
Medical Devices
CDSCO registration, import licenses, and market authorization for Class A–D devices.
Drugs & Pharmaceuticals
Drug registration, manufacturing licenses, clinical trial approvals through CDSCO.
In-Vitro Diagnostics
IVD product registration and compliance under India's evolving IVDR framework.
Biologicals
Regulatory pathways for vaccines, blood products, and biosimilars.
Cosmetics
CDSCO cosmetic registration, import licenses, and cosmetovigilance compliance.
Food Products
FSSAI licensing, food safety compliance, labeling regulations, and import clearance.
Agrochemicals
Registration of insecticides, pesticides, and home care products under CIB&RC.
Home Products
BIS certification, Legal Metrology compliance, and EPR registration for consumer products.
What We Do
Comprehensive Regulatory Solutions
Three pillars of expertise that cover the full lifecycle of regulatory compliance in India.
Core Capability
Regulatory Affairs & Licensing
End-to-end regulatory support across 15+ Indian regulatory bodies including CDSCO, FSSAI, BIS, DGFT, WPC, and more. We handle product registration, manufacturing licenses, import permits, and ongoing compliance — so you can focus on your business.
- CDSCO drug & device registration
- FSSAI food business licensing
- BIS product certification
- Import/export permits (DGFT, SIP)
- Legal Metrology & EPR compliance
Safety & Compliance
Pharmacovigilance & Vigilance Services
Comprehensive post-market surveillance and safety monitoring services. Our vigilance teams ensure your products maintain compliance throughout their lifecycle — covering drugs, devices, cosmetics, and food products.
- Pharmacovigilance (drug safety monitoring)
- Materiovigilance (medical device reporting)
- Cosmetovigilance & food safety vigilance
- Adverse event reporting & PSUR management
Clinical Development
Clinical Trials & Field Studies
From protocol development to ICMR/DCGI approvals, we manage the full clinical trial lifecycle in India. Our team navigates the regulatory requirements so your studies run on time and within compliance.
- Clinical trial regulatory approvals
- ICMR & Ethics Committee coordination
- Field safety trials for agrochemicals
- Post-market clinical follow-up (PMCF)
Regulatory Bodies We Work With
CDSCO
Central Drugs Standard Control Organization
FSSAI
Food Safety and Standards Authority of India
BIS
Bureau of Indian Standards
DGFT
Directorate General of Foreign Trade
WPC
Wireless Planning & Coordination
CIB&RC
Central Insecticides Board
PESO
Petroleum and Explosives Safety Organisation
LMPC
Legal Metrology
ISO 9001:2015
Certified Quality Management