TEPA Intelligence Tool
Compliance Checklist Generator
Step-by-Step Export Compliance
Enter your HS code — get your full checklist
Generates a personalised export compliance checklist: TEPA origin documentation, sector-specific Indian regulatory requirements (CDSCO / FSSAI / BIS), and the 6-step customs clearance process. Print or save as PDF.
TEPA Export Compliance Checklist
HS Code 3004
Generated by India Market Intelligence Platform · 3/17/2026
0 of 12 items completed
0%
TEPA Concession — HS 3004
MFN BCD
10%
TEPA Staging
E5
Description
Penicillins
1. TEPA Origin Documentation
EUR.1 Movement CertificateREQUIRED
Issued by Swiss customs (BAZG/OFDF) — certifies TEPA origin. Required for all TEPA preferential claims.
Origin Declaration on Invoice
For shipments ≤ EUR 6,000, an approved exporter may use an invoice declaration instead of EUR.1.
Approved Exporter Status
Apply to Swiss customs for approved exporter status to use invoice declarations for shipments > EUR 6,000.
Long-Term Supplier Declaration
If using materials from multiple Swiss suppliers, obtain LTSDs from each to support the EUR.1.
2. Indian Import Process (6 Steps)
Step 1: Obtain IEC (Import Export Code)1–3 days
Indian importer must hold a valid IEC from DGFT. Apply online at dgft.gov.in. Free of charge.
Step 2: Sector-Specific RegistrationVaries by sector
Complete the regulatory registration for your product category (CDSCO / FSSAI / BIS — see above).
Step 3: Obtain EUR.1 Certificate1–5 working days
Swiss exporter applies to BAZG (Swiss Federal Customs Administration) before shipment. Certificate is valid for 10 months.
Step 4: Prepare Commercial InvoiceBefore shipment
Invoice must state: HS code, country of origin (Switzerland), TEPA preferential claim, and EUR.1 reference number.
Step 5: Customs Filing (Bill of Entry)At port of entry
Indian importer files Bill of Entry on ICEGATE portal. Select 'TEPA preferential rate' and attach EUR.1.
Step 6: Port Clearance & Duty Payment1–5 working days
Customs assesses duty at TEPA preferential rate. Pay any remaining duty (if staged, not yet 0%). Goods released.
3. Sector Regulatory Requirements — CDSCO
Registration: Drug Registration (Form 40/41)
Estimated timeline: 12–18 months
Manufacturing licence (Form 25/28)
GMP certificate (WHO/EU)
Certificate of Pharmaceutical Product (CoPP)
Stability data (ICH Q1A)
Clinical trial data (if applicable)
Disclaimer: This checklist is for guidance only. Regulatory requirements change frequently. Always verify with a licensed Indian customs broker, the relevant regulatory authority (CDSCO/FSSAI/BIS), and Swiss customs (BAZG) before shipping. TEPA concession data is from the official EFTA–India TEPA schedules.