Efficient management of foreign-trade registrations, authorisations and export documentation helps pharmaceutical and healthcare businesses navigate India's evolving import-export requirements and avoid unnecessary delays in international trade.
What We Deliver
- Importer Exporter Code (IEC) — Assistance with new IEC applications, modifications, updates and related DGFT requirements.
- Advance Authorisation — Application and documentation support for Advance Authorisation schemes for eligible imports linked to export obligations.
- DGFT Application & Amendment Support — Preparation and submission support for applicable DGFT applications, amendments and regulatory requests.
- Export Documentation & Compliance — Assistance with documentation and regulatory requirements associated with pharmaceutical and healthcare product exports.
- Free Sale / Export Certificates — Regulatory support and coordination for applicable Free Sale Certificates and other export-related certificates through the relevant authority.
- Certificate of Pharmaceutical Product (CoPP) / Export Regulatory Support — Support for applicable export-related pharmaceutical regulatory documentation and coordination with the relevant regulatory authority.
- DGFT Correspondence & Clarifications — Assistance with responses, clarifications and documentation requested in connection with DGFT applications.
- Export Authorisation & Compliance Support — Support for applicable export authorisations, documentation and compliance requirements based on the product and destination.
Our Approach
Assess
We understand your product, export model, destination markets and applicable foreign-trade requirements.
Prepare
We identify the applicable authorisation, registration and supporting documentation requirements.
File & Follow Up
We prepare and submit the applicable applications and coordinate responses to regulatory queries.
Maintain Compliance
We support amendments, renewals, export documentation and ongoing compliance requirements as applicable.
Who this is for
DGFT & Allied Export Regulatory Support
While DGFT manages India's foreign-trade framework and related authorisations, certain product-specific certificates and regulatory approvals are issued by other competent authorities. Vaayath provides coordinated support across the applicable regulatory pathways to help exporters complete the required documentation efficiently.
Pharmaceutical Export Regulatory Support
Pharmaceutical exports may involve multiple regulatory and trade requirements beyond basic DGFT registration. Vaayath provides coordinated support for applicable DGFT requirements alongside product-specific regulatory documentation and certificates required by the relevant Indian authorities and destination markets.
IEC & DGFT Registration
Importer Exporter Code registration, profile updates and DGFT licensing support.
Advance Authorisation
Duty-free import scheme support linked to export obligations.
Export Certificates
CoPP, GMP certificates and export regulatory documentation.
Free Sale Certificate
Coordination and issuance support through competent Indian regulatory authorities.