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Indonesia

Regulatory Affairs Update: Indonesia

Indonesia: Implementation of GDPMD Certificate (CDAKB: Cara Distribusi Alat Kesehatan yang Baik) as a Requirement for Marketing Authorization

May 9, 2024

Regulatory Affairs Update Indonesia

Indonesia: Decree Of The Minister Of Health Of The Republic Of Indonesia Number HK.01.07/Menkes/163/2024 About Consolidated Display on Sectoral Electronic Catalogue

April 9, 2024

Regulatory Affairs Update: Philippines

Philippines: Extension of the Regulatory Flexibility for Class B, C, and D Medical Devices that are not Included in the List of Registrable Medical Devices Based on FDA Circular No. 2020-001-A

April 3, 2024

Regulatory Affairs Update: Indonesia

Indonesia: Listing Product Schedule Update in the Ministry of Health e-Catalogue

April 2, 2024

Regulatory Affairs Update Indonesia

Indonesia: Announcement of the Listing Product Schedule Update in e-Catalogue Ministry of Health

March 20, 2024

Scientist working in laboratory

Indonesia: List Of SNI ISO/IEC 17025:2017 Accredited Testing Laboratories For Medical Devices And Household Supplies In Indonesia

December 14, 2023

Person tapping on a padlock icon

Indonesia: Temporary Closing of the Online System for Submission of Medical Devices and Household Supplies Registration, Online Certificates, and Distribution License by the Ministry of Health of Indonesia

December 14, 2023

Two scientists wearing PPE

Indonesia: Procedure for the Implementation of Foreign Halal Certificate Registration by The Halal Product Guarantee Administering Agency (BPJPH) in Indonesia

December 14, 2023

Person looking at big virtual calendar

Indonesia: Draft of Government Regulations concerning the Implementation of Law No. 17 of 2023 concerning Health in Indonesia

December 14, 2023

LED board showing shopping cart icons

Indonesia: Procedure on Substitution of Imported Medicines and Medical Devices with Domestic Medicines and Medical Devices in the Sectoral e-Catalogue of the Ministry of Health of Indonesia

November 3, 2023

Certification Cost of Device Certification

Indonesia: Cost of Device Certification according to Government Regulation No. 43 Year 2023

October 10, 2023

Indonesia: Government Goods/Services Procurement Policy Agency (LKPP: Lembaga Kebijakan Pengadaan Barang/Jasa Pemerintah) issued an Announcement Letter about Brand Integration in e-Catalogue

October 9, 2023

Indonesia’s Government Issued a New Regulation Pertaining to Health

September 11, 2023

Indonesia: Ministry of Communication and Informatics (Kominfo) proposed changes on the standards for Telecommunication Equipment and/or Equipment Short Distance Telecommunications Devices

August 8, 2023

Indonesia’s Halal Regulation Update

August 2, 2023

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ANDAMAN MEDICAL PTE LTD (Registration no. 201524804D)
(Head Office Singapore)
Tampines Junction Business Center
Level 09-02 300 Tampines Avenue 5, Singapore 529653

ANDAMAN MEDICAL PTE LTD
(Registration no. 201524804D)
(Head Office Singapore)
Tampines Junction Business Center Level
09-02, 300 Tampines Avenue 5, Singapore 529653

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sales@andamanmed.com

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Welcome to Andaman Medical. We are your trusted partner for regulatory affairs and market access in Southeast Asia.

Whether you are a medical device manufacturer or distributor, our dedicated team is here to help you navigate the complex regulatory landscape and bring your products to market efficiently and compliantly.

Main Pages

Home
About Us
Services
Contact Us

Address

ANDAMAN MEDICAL PTE LTD (Registration no. 201524804D)
(Head Office Singapore)
Tampines Junction Business Center
Level 09-02 300 Tampines Avenue 5, Singapore 529653

ANDAMAN MEDICAL PTE LTD
(Registration no. 201524804D)
(Head Office Singapore)
Tampines Junction Business Center Level
09-02, 300 Tampines Avenue 5, Singapore 529653

E-mail Address

sales@andamanmed.com

Phone Number

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