Secure Export No Objection Certificates (NOCs) for pharmaceuticals, new drugs, unapproved drugs, banned drugs, APIs, and other regulated products with complete documentation support, regulatory strategy, and end-to-end coordination with CDSCO.
What We Deliver
- Export NOC Eligibility Assessment — Determine whether your product requires an Export NOC and identify the applicable regulatory pathway.
- Documentation Review — Preparation and review of Covering letters, Purchase orders, Undertakings, Product details, Manufacturing licences, Export permissions, Supporting declarations
- CDSCO Online Filing — Application preparation, Upload of supporting documents, Application validation
- Regulatory Strategy — Guidance for Unapproved drugs, Banned drugs, New drugs
- Deficiency Management — Review deficiency letters, Prepare clarifications, Submit revised documents, Technical justifications, Authority follow-up
Documents Required
Our Approach
Eligibility Assessment
Review the product category, applicable regulations, and determine the Export NOC requirements.
Documentation Preparation
Prepare and verify all required documents, declarations, undertakings, and supporting information.
Application Filing & Follow-up
Submit the application through the applicable CDSCO portal and coordinate with regulatory authorities until a decision is issued.
Export Readiness Support
Assist with clarification requests, amendments, additional approvals, and future Export NOC requirements.