Import of certain drugs, chemicals and pharmaceutical substances for industrial, research, veterinary, cosmetic or other non-medicinal purposes requires a Dual Use Licence from CDSCO. Vaayath assists importers, manufacturers and traders in determining eligibility, preparing documentation, filing applications and obtaining approvals with minimal regulatory delays.
What We Deliver
- Product Eligibility Assessment — Determine whether the imported substance requires a Dual Use Licence and evaluate the applicable regulatory pathway.
- Documentation Preparation — Preparation and review of undertaking, end-use declaration, technical documents and supporting information.
- Application Filing — Preparation and submission of Dual Use Licence applications through the applicable CDSCO portal.
- Regulatory Liaison — Coordination with CDSCO for clarification, deficiency responses and approval follow-up.
- Import Compliance Guidance — Advice regarding conditions of licence, customs documentation and post-approval compliance.
- Renewal & Amendment Support — Support for amendments in importer details, products, quantity or end-use.
Our Approach
01
Initial Assessment
Review product composition, intended use and import purpose to determine licence applicability.
02
Documentation
Prepare declarations, technical documents and supporting evidence.
03
Application Submission
Submit application through CDSCO and coordinate with regulatory authorities.
04
Approval & Import Support
Assist until licence issuance and provide guidance during import clearance.
Who this is for
Importers of PharmaceuticalsChemical ManufacturersResearch LaboratoriesCosmetic ManufacturersVeterinary Product CompaniesAPI TradersBiotechnology Companies
Why Choose Vaayath
- 20+ years of CDSCO regulatory experience
- End-to-end documentation support
- Expertise in import licensing
- Deficiency response preparation
- Faster regulatory coordination
- Support for domestic and overseas clients