Regulatory & Commercial Compliance Solutions
Strategic regulatory, compliance and commercial support across the entire product lifecycle—from development and approvals to manufacturing, market access and post-approval compliance.
Navigating India's evolving regulatory landscape requires technical expertise, regulatory insight and practical execution. Vaayath provides end-to-end regulatory and compliance support to pharmaceutical, medical device and cosmetic companies—from regulatory strategy and dossier preparation to licensing, authority interactions, GMP compliance and post-approval requirements.
We help regulated businesses navigate the requirements to enter, operate and remain compliant in the Indian market. Explore the individual services below.
Pharmacovigilance Services
Comprehensive pharmacovigilance support covering PV system implementation, ADR monitoring, ICSR processing, PSUR/PBRER preparation, signal monitoring and regulatory reporting to support ongoing product safety and compliance.
NPPA Compliance & IPDMS Services
End-to-end support for NPPA/DPCO compliance, price notifications, IPDMS registration and submissions, Form II and Form V filings, price revision, regulatory correspondence and pricing-related compliance matters.
DGFT Services
End-to-end support for Importer Exporter Code (IEC), Advance Authorisation, export documentation, Free Sale Certificate coordination, DGFT applications and amendments, and other foreign trade compliance requirements.
FSSAI Relabeller License and Compliance Services
End-to-end support for FSSAI relabeller licensing, renewals, modifications, manufacturer linkages, annual returns, label compliance and ongoing food regulatory requirements.
Why Choose Vaayath?
Regulatory Expertise
Practical regulatory experience across pharmaceuticals, medical devices, cosmetics and allied regulated products.
Authority-Focused Approach
Support for regulatory submissions, deficiencies, authority communications, inspections and post-approval requirements.
End-to-End Support
From regulatory strategy and documentation to approvals, compliance and lifecycle management.
Inspection & Compliance Expertise
GMP audit, inspection readiness, gap assessment, CAPA and remediation support.
Cross-Functional Expertise
Integrated regulatory, quality, pharmacovigilance, legal and commercial compliance support.
India & Global Regulatory Support
Supporting manufacturers, importers and businesses navigating Indian and international regulatory requirements.
Regulatory Expertise at Scale
Experience across CDSCO, WHO, USFDA, MHRA, Health Canada, TGA, ANVISA and other international regulatory environments.
Frequently Asked Questions
Ready to navigate regulatory complexity with confidence?
Whether you are launching a new product, expanding manufacturing capabilities, preparing for a regulatory inspection or addressing a compliance challenge, our experts are ready to help you plan, prepare and execute with confidence.