COMPLIANCE MAP

Global Reach. Local Compliance

Wherever you operate, our regularly updated map will guide you to full regulatory compliance.

Poland

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Latvia

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

United States

Regulation name:

DSCSA enacted

Serialization status:

Active

China

Regulation name:

National Medical Products Administration

Serialization status:

Active

Azerbaijan

Regulation name:

Law of the Republic of Azerbaijan on Medicinal Products

Serialization status:

In progress

Bahrain

Regulation name:

Bahrain NHRA Regulation

Serialization status:

Active

Saudi Arabia

Regulation name:

Saudi Arabia SFDA Compliance

Serialization status:

Active

Russia

Regulation name:

Federal Law No. 488-FZ

Serialization status:

Active

Kazakhstan

Regulation name:

Order No. 453: On Approval of the Rules for the Labeling and Traceability of Medicinal Products

Serialization status:

Active

Kyrgyzstan

Regulation name:

Serialization status:

Active

Uzbekistan

Regulation name:

Uzbekistan Govt. Decree No.737

Serialization status:

Mandatory

India

Regulation name:

India iVEDA Compliance

Serialization status:

Required for drug exports

Australia

Regulation name:

TGO 106

Serialization status:

Active

Canada

Regulation name:

Serialization status:

Not mandatory

Philippines

Regulation name:

Serialization status:

On hold

Indonesia

Regulation name:

BPOM Regulation No.33 of 2018 on the Application of 2D Barcodes for Food and Drug Control

Serialization status:

In progress

South Korea

Regulation name:

SOUTH KOREAN SERIALIZATION REGULATION

Serialization status:

Active

Austria

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Belgium

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Bulgaria

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Cyprus

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Czechia

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Denmark

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Finland

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Estonia

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

France

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Germany

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Croatia

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Hungary

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Iceland

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Ireland

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Liechtenstein

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Lithuania

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Luxembourg

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Malta

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Netherlands

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Norway

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Portugal

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Romania

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Slovakia

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Spain

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Sweden

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Switzerland

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Italy

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

Greece

Regulation name:

EU Falsified Medicines Directive

Serialization status:

Active

United Kingdom

Regulation name:

Serialization status:

EU FMD no longer applies to the United Kingdom.

Egypt

Regulation name:

Egyptian Pharmaceutical Track & Trace System (EPTTS)

Serialization status:

Barcoding mandatory since 2022

Algeria

Regulation name:

National Agency for Pharmaceutical Products traceability mandate

Serialization status:

Initiated in 2025

Ethiopia

Regulation name:

Ethiopian Pharmaceutical Products Traceability Directive (No. 43/2019) and EFDA Traceability Master Data Guideline

Serialization status:

Phased implementation (2022–2027)

Libya

Regulation name:

Decision No. 379/2023 on Pharmaceutical & Medical Device Serialization

Serialization status:

Mandatory serialization since January 2024

Zambia

Regulation name:

Zambia Pharmaceutical Traceability Guideline 2023 (ZAMRA)

Serialization status:

Serialization system under development

Nigeria

Regulation name:

NAFDAC Pharmaceutical Products Traceability Regulations

Serialization status:

No national serialization mandate

Ghana

Regulation name:

Ghana Pharmaceutical Traceability Strategy (2022) & FDA traceability guidelines (2023)

Serialization status:

No serialization law; anticounterfeit measures in place

Kenya

Regulation name:

Pharmacy and Poisons Board (PPB) Pharmaceutical Traceability Initiative (in development)

Serialization status:

Developing serialization framework

Morocco

Regulation name:

Draft national pharmaceutical traceability regulation (under development, not yet enacted)

Serialization status:

Serialization regulations under discussion

Tunisia

Regulation name:

No national serialization law; companies voluntarily exploring GS1 serialization (e.g., UNIMED & Laboratoires MédiS) for export compliance

Serialization status:

Exploring serialization implementation

South Africa

Regulation name:

Government Notice No. 988 of 2017 (NDoH) and SAHPRA serialization guidelines (2022–2024)

Serialization status:

No national serialization mandate

Central Africa

Regulation name:

Central Africa Track & Trace Framework

Serialization status:

Regional implementation underway

SADC Region

Regulation name:

SADC Regional Pharmaceutical Traceability Harmonization Initiative

Serialization status:

Progressive adoption across member states

Argentina

Regulation name:

Resolution 435/2011 – Argentina National Drug Traceability System

Serialization status:

Active

Brazil

Regulation name:

RDC 157/2017, Law 13.410/2016 – National Medicine Control System (SNCM)

Serialization status:

In progress but effectively suspended

Chile

Regulation name:

Pilot programs only (no national law yet) – e.g., voluntary GS1 pilots under ANAMED/ISP oversight

Serialization status:

Colombia

Regulation name:

Voluntary pilot initiatives (GS1 traceability system under INVIMA); Law 1122/2007 mandates traceability framework but no mandatory serialization yet

Serialization status:

Ecuador

Regulation name:

ARCSA-DE-030-2020-MAFG (replaced by ARCSA-DE-010-2021-LDSS)
 

Serialization status:

Paraguay

Regulation name:

Decree 2479/24 (Sep 2024) – updates Law 1119/97 for registration and labeling; Decree 2942/2024

Serialization status:

Peru

Regulation name:

Legislative Decree No. 1161 (Law on Health Products), Supreme Decree No. 016-2011-SA (DIGEMID regulation)

Serialization status:

Uruguay

Regulation name:

Decree 324/999 & Decree 38/015 regulate medical devices and biologics; no traceability decree currently in place

Serialization status:

Bolivia

Regulation name:

Ley N° 1737 (1996), Decreto Supremo N° 25235 (1998); no current decree on serialization or traceability

Serialization status:

Venezuela

Regulation name:

Ley Orgánica de Salud (1998); no decree mandating serialization or traceability

Serialization status:

Jordan

Regulation name:

JFDA Implementation Guideline for Barcode Labeling of Prescription Drugs

Serialization status:

Serialization on secondary packaging required; extended deadline: June 30, 2025

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Vitold
CEO of Nubinno connect.

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