vitality pharma navigator is a leading consultancy firm providing a comprehensive range of professional regulatory services across all major and minor domains.
Our clients receive outstanding value through high-quality, affordable, personalized, and prompt regulatory services. We accept accountability for the success of every project and work to build lasting relationships focused on finding solutions.
From pharmaceuticals to food products, we provide end-to-end regulatory support across every major product category in India.
CDSCO registration, import licenses, and market authorization for Class A–D devices.
Drug registration, manufacturing licenses, clinical trial approvals through CDSCO.
IVD product registration and compliance under India's evolving IVDR framework.
Regulatory pathways for vaccines, blood products, and biosimilars.
CDSCO cosmetic registration, import licenses, and cosmetovigilance compliance.
FSSAI licensing, food safety compliance, labeling regulations, and import clearance.
Registration of insecticides, pesticides, and home care products under CIB&RC.
BIS certification, Legal Metrology compliance, and EPR registration for consumer products.
Three pillars of expertise that cover the full lifecycle of regulatory compliance in India.
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
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
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)
Central Drugs Standard Control Organization
Food Safety and Standards Authority of India
Bureau of Indian Standards
Directorate General of Foreign Trade
Wireless Planning & Coordination
Central Insecticides Board
Petroleum and Explosives Safety Organisation
Legal Metrology
Certified Quality Management
