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Japan PMDA & JAS Guide — India Exporters

190 words · 28 sections · 1 data table(s)

Market: Japan | Scope: 30, 20, 84

REGULATORY ENTRY GUIDES

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Regulatory Overview

Key Regulatory Requirements

Primary legislation and regulatory authority for this market

Registration, licensing, or certification required before market entry

Ongoing compliance obligations post-market-entry

Labelling, marking, and language requirements

Import permit or quota requirements where applicable

Step-by-Step Market Entry

Identify applicable regulations and competent authority

Classify product under correct HS code — determines regulatory pathway

Engage local regulatory consultant / CHA for this market

Complete product registration / notification as required

Obtain import licence / quota / prior approval if needed

Ensure labelling and packaging compliance before shipment

File import declaration and pay applicable duties

Common Regulatory Pitfalls

Wrong regulatory pathway chosen — pharmaceutical vs food vs cosmetic classification

Expired or non-recognised certification body used

Missing local agent/importer registration (required in many markets)

Labelling non-compliance — language, font size, mandatory warnings

Inadequate post-market surveillance and adverse event reporting

AJG Regulatory Intelligence

This guide is part of AJG's 184-country regulatory intelligence database. All mandates facilitated commission-only — no retainer.

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ParameterDetails
Guide TitleJapan PMDA & JAS Guide — India Exporters
Target MarketJapan
Applicable Sectors30, 20, 84
Key RegulationsPMDA (pharma), JAS (agro), PSE (electronics), METI notification
AJG ApplicationCommission-only mandate facilitation in regulated markets

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