Global Food Compliance
Intelligence & Solutions
Home / News / Details

Malaysia Issues Halal Certification Procedure for International Manufacturing

According to the Halal Malaysia Official Portal, effective from January 1, 2024, the application process for Malaysian Halal Certification for International Manufacturing must be in line with the procedure outlined in the official announcement1 issued on December 22, 2023.

The application is opened for companies registered in Malaysia. Eligible applicants for the Halal Certificate fall into the following categories:

  • Branches

  • Subsidiaries companies

  • Importers

  • Distributors/traders

  • Agents in Malaysia

Applicants are required to prepare the application form (available here) along with the following documents.

No.

Needed documents

1

Cover letter of the application, which explains;

a) Brief information on the application; and

b) Summary of raw materials/ingredients

2

Registration of company in Malaysia

3

Manufacturing license from the local authority (for international manufacturer)

4

Halal Executive certificate and the appointment letter for halal Executive (manufacturer and/or applicant);

*Halal Executive must be Muslim

5

Copy of identity card and the appointment letter for two Muslim workers (if any)

6

Halal Assurance System (HAS) as below (Manufacturer and/or applicant);

a)  For first-time application and/or new manufacturer:

-   Halal Assurance System Manual/Procedure

b)  For renewal and/or existing manufacturer:

-   Halal Policy

-   Internal Halal Committee

-   Summary of Halal Risk Management Plan

-   HAS amendment (if any)

7

Halal certificate or product specification for all raw materials or ingredients;

a)  Documents should be compiled according to the list of raw materials in the MYeHALAL system; and

b)  Raw materials must be clearly marked on the halal certificate or related documents

8

Halal certificate or product specification for processing aids including water filter/purification used in the factory;

9

Manufacturing license from National Pharmaceutical Regulatory Agency (NPRA) (for pharmaceutical and cosmetic products only) (if applicable); 

10

Establishment license, medical device registration from Medical Device Authority (MDA) and ISO 13485:2017 (for medical device products only) (if applicable);

11

Flow chart of product processing;

12

Packaging artwork;

13

Factory layout plan;

14

Factory location map; 

15

Other documents of manufacturers such as Halal Certificate, HACCP, ISO, GHP, GMP, TQM, etc. (if applicable)

Following the submission of applications, if everything proceeds smoothly, an audit will be conducted at the manufacturing plant. The audit duration will be a minimum of four days and limited to one manufacturing address. Additionally, one application form can only be used for the application of one factory, and can be used for the registration of a maximum of 100 products. All certifications are valid for two years.

Please note that for abattoir and meat-based product applications, enterprises should contact the Department of Veterinary Services for further information. For more details, please refer to the official announcement.

We provide full-scale global food market entry services (including product registration, ingredient review, regulatory consultation, customized training, market research, branding strategy). Please contact us to discuss how we can help you by [email protected]
Copyright: unless otherwise stated all contents of this website are ©2026 - REACH24H Consulting Group - All Rights Reserved - For permission to use any content on this site, please contact [email protected]
User Guide