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Monday 08:00 - 17:00 Tuesday 08:00 - 17:00 Wednesday 08:00 - 17:00 Thursday 08:00 - 17:00 Friday 08:00 - 17:00

Sixmurs Perdana PT

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Sixmurs Perdana PT

Contact information, map and directions, contact form, opening hours, services, ratings, photos, videos and announcements from Sixmurs Perdana PT, Medical and health, The Kensington Office Tower Lantai 11, Jalan Boulevard Raya No. 1, Kelapa Gading, Jakarta.

Sixmurs Group of company, aims to help clients to focus and excel in their core businesses by providing essential services such as consulting, license holding, trading, importation, logistic, manufacturing etc.

16/01/2026

Isra Miraj Mubarak 🌙
May the journey of Isra Miraj inspire reflection, steadfast faith, and renewed semangat in serving a greater purpose.
As we continue our mission to strengthen compliant healthcare infrastructure across Southeast Asia, may this blessed occasion remind us of the importance of integrity, responsibility, and positive impact for communities we serve.

01/01/2026

Happy New Year 2026! ✨️

Welcoming 2026 with renewed purpose and passion. Thank you to our partners for your continued trust as we build compliant healthcare infrastructure for growth across Southeast Asia.

May this new year bring us closer to better healthcare in Southeast Asia 🩺

25/12/2025

Merry Christmas!
Wishing you joy, peace, and good health this festive season.

May your days be filled with warmth, hope, and togetherness.

16/12/2025

The upcoming Malaysia–Thailand Regulatory Reliance Pilot could change how fast medical devices enter both markets.
If your device is already registered in either country, this pathway may open a much quicker route for your next submission.

Here is what you need to know before the pilot begins in February 2026. ↓

HealthcareIndustry
ASEANHealthcare

12/11/2025

Happy National Health Day!
We continue to empower healthcare brands through compliance and quality for safer communities.

21/07/2025

Can labeling your device as "Research-Use-Only" help you enter Indonesia faster?
Many medical device brands ask this when planning early market entry. But RUO is not a shortcut. It is a strategic tool, and using it the wrong way can put your brand at risk.

In this post, we explain:
✔️ What RUO really means
✔️ When it can help and when it cannot
✔️ How to stay compliant while building early presence

If you are planning to enter Indonesia in 2025 or preparing your product for licensing, this is essential reading.

👉 Learn how to navigate RUO and full licensing paths the right way.
Join our expert webinar on July 30. Event details in the last slide.

21/10/2022

GUIDELINE FOR RE-REGISTRATION OF REGISTERED MEDICAL DEVICE
September 2022 Second Edition

To provide information and explanation to the establishment on how to submit re-registration of registered medical device application under Act 737 and MDR 2012.
These are some of the information that have been updated in the 2nd edition of Medical Device 2022 updates and there are many more, some of the updates are as below:
• Re-registration Stages of Registered Medical Device
Stage 1: Application for conformity assessment conducted by Conformity Assessment Body (CAB)
Stage 2: Application for re-registration of medical device via MeDC@St.
• Re-registration Requirement and Process Flow
• Payment Information
• Fee Information
For more information and guidance, you may approach a Regulatory Affairs Specialist at Sixmurs Malaysia to guide you accordingly. Don’t hesitate to contact us at info@sixmurs.com or www.my.sixmurs.com.

26/08/2022

DRUG REGISTRATION GUIDANCE DOCUMENT (DRGD) THIRD REVISION JULY 2022

DRGD will serve as the reference guide for the registration process including quality control, inspection & licensing and post registration activities of medicinal products.

These are some of the information that have been updated in the 3rd edition of DRGD July 2022 updates and there are many more, some of the updates are as below:
• Amendment of Section E: Post-Registration Process
• Amendment of Appendix 18: List of Permitted, Prohibited and Restricted Substances
• Amendment of Appendix 20: Specific Labelling Requirements
• Amendment of Appendix 27: Inspection
• Addition of new ingredient 44. Chloroquine and Hydroxychloroquine and safety information
• The specific labelling requirements for existing ingredient

For more information and guidance, you may approach Regulatory Affairs Specialist at Sixmurs Malaysia to guide you accordingly.

16/08/2022

All Board of Directors and Employees of PT Sixmurs Perdana wish you Happy Independence Day of the 77th Republic of Indonesia, recover faster to rise stronger!

01/08/2022

Good news for medical device distributors in Indonesia…

Indonesia Ministry of Health launched an acceleration program for CDAKB (Cara Distribusi Alat Kesehatan yang Baik) certification which is dedicated for medical device distributor that own SDAK (Sertifikat Distribusi Alat Kesehatan) or IDAK (Izin Distribusi Alat Kesehatan). Medical device distributors joining this program will be prioritized to get CDAKB mentoring program by MoH Medical Device Surveillance, besides, they may obtain CDAKB certificate without having an on-site audit (with specific terms and conditions).
Just by accessing and completing the form provided in the above brochure, medical device distributors that are interested in this program can participate.

Please do not hesitate to contact our professional team at info@sixmurs.com or visit for more detailed information on requirements, processes, and other related information.

(Source: https://sertifikasialkes.kemkes.go.id/index.php /berita/146)

29/07/2022

Sixmurs Perdana group of companies wishing you Happy Islamic New Year 1 Muharram 1444H.

28/07/2022

Legalization of Foreign Public Documents for Cosmetic Notification Submission⁣
⁣
The Deputy for Supervision of Traditional Medicines, Health Supplements, and Cosmetics issued Circular Letter Number HK.07.4.41.07.22.14 concerning Legalization of Foreign Public Documents for Cosmetic Notification submission as an alignment with the Government Regulation Number 2 Year 2021 about the Approval of Convention Abolishing the Requirement of Legalization for Foreign Public Documents. ⁣
⁣
With the issuance of this circular, legalization of foreign public documents from countries member of the convention will be caried out through apostille mechanism including documents that are needed for cosmetic notification of imported products. The apostille certificate will be valid to replace the legalization of Certificate of Free Sales (CFS) and/or Good Manufacturing Practice (GMP) by Republic of Indonesia Embassy to fulfill the cosmetic notification requirement.⁣
⁣⁣
Please do not hesitate to contact our professional team at info@sixmurs.com for more detailed information on requirements, processes, and other related information.
⁣
(Source: SE Legalisasi Dokumen Publik Asing)

Address

The Kensington Office Tower Lantai 11, Jalan Boulevard Raya No. 1, Kelapa Gading
Jakarta
14240

Opening Hours

Monday	08:00 - 17:00
Tuesday	08:00 - 17:00
Wednesday	08:00 - 17:00
Thursday	08:00 - 17:00
Friday	08:00 - 17:00

Telephone

+628119635222

Website

https://www.sixmurs.com/

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