Pharma Regulatory Services

Export NOC Services

Expert Assistance for CDSCO Export NOC Applications. Exporting pharmaceutical products from India often requires obtaining a No Objection Certificate (NOC) from the Central Drugs Standard Control Organization (CDSCO), particularly for unapproved drugs, new drugs and banned drugs. Our experts assist with eligibility assessment, documentation preparation, online filing, authority correspondence, and follow-up to help ensure timely issuance of Export NOCs and uninterrupted international shipments.

20+ Years Regulatory Experience
CDSCO Export Experts
100% Success Rate
PAN India Support

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

Manufacturing Licence
Product Permission
Purchase Order
Commercial Invoice (where applicable)
Product Composition
Undertaking
Country Requirements
Product Labels
Export Details
Authorization Letter
Other supporting documents as required by CDSCO

Our Approach

01

Eligibility Assessment

Review the product category, applicable regulations, and determine the Export NOC requirements.

02

Documentation Preparation

Prepare and verify all required documents, declarations, undertakings, and supporting information.

03

Application Filing & Follow-up

Submit the application through the applicable CDSCO portal and coordinate with regulatory authorities until a decision is issued.

04

Export Readiness Support

Assist with clarification requests, amendments, additional approvals, and future Export NOC requirements.

Who this is for

Pharmaceutical ManufacturersAPI ManufacturersExportersMerchant ExportersThird-Party ManufacturersContract ManufacturersMarketing Authorization HoldersForeign Buyers Procuring from India

Products Covered

Finished Formulations
Active Pharmaceutical Ingredients (APIs)
New Drugs
Unapproved Drugs
Banned Drugs
Export-only Products

Frequently asked questions

Let's Talk

Export Globally with Regulatory Confidence

Obtaining an Export NOC is a critical regulatory requirement for many pharmaceutical products intended for international markets. Incomplete documentation, incorrect product classification, or procedural deficiencies can result in delays that affect shipment schedules and customer commitments. At Vaayath, we provide end-to-end regulatory support for Export NOC applications—from eligibility assessment and documentation preparation to online filing, regulatory follow-up, and post-approval assistance. Our experienced team works closely with manufacturers and exporters to ensure applications are complete, compliant, and processed efficiently. Partner with Vaayath to streamline your Export NOC applications and ensure smooth global shipments with confidence.