Vietnam

What Japanese Manufacturers Need to Know About Vietnam Cosmetics Registration

From registration to tariffs and CPTPP benefits, here’s what Japanese cosmetics manufacturers need to know about Vietnam’s cosmetics market.

July 9, 2026
What Japanese Manufacturers Need to Know About Vietnam Cosmetics Registration
How to Meet Vietnam Medical Device Dossier Requirements for Registration

Learn how to prepare a compliant dossier for Vietnam medical device registration in this guide for foreign manufacturers.

July 9, 2026
How to Meet Vietnam Medical Device Dossier Requirements for Registration
How the Vietnam Medical Device Change Notification Process Works

Learn how to manage medical device renewals, variations, and change notifications in Vietnam with step-by-step MOH submission guidance.

July 9, 2026
How the Vietnam Medical Device Change Notification Process Works
What Are the Medical Device Renewal Timelines Across ASEAN?

Learn about license validity and renewal rules for medical devices in Southeast Asia.

July 9, 2026
What Are the Medical Device Renewal Timelines Across ASEAN?
What's the Difference? Fast-Track vs Standard Medical Device Registration in Vietnam

Explore Vietnam’s fast-track and standard medical device registration pathways and the role of reference approvals in shortening timelines.

July 9, 2026
What's the Difference? Fast-Track vs Standard Medical Device Registration in Vietnam
How to Fast-Track Medical Device Registration in Southeast Asia

Explore fast-track medical device registration in Southeast Asia, cut timelines by 6–12 months, and accelerate market entry with Cisema.

July 9, 2026
How to Fast-Track Medical Device Registration in Southeast Asia
What Is the Vietnam Cosmetic Product Registration and Notification Process?

Cosmetic product registration and notification in Vietnam involves specific processes, fees, and timelines under the ASEAN Cosmetic Directive.

July 9, 2026
What Is the Vietnam Cosmetic Product Registration and Notification Process?
Understanding the ASEAN Medical Device Market: Malaysia, Singapore, & Vietnam

Learn how to fast-track medical device registration in ASEAN: timelines, costs, and license options in Malaysia, Singapore, and Vietnam.

July 9, 2026
Understanding the ASEAN Medical Device Market: Malaysia, Singapore, & Vietnam
Explained: How Vietnam Medical Device Registration Works (Timelines, Fees, & AR Strategy)

Gain an overview of the medical device registration process in Vietnam with timelines, fees, and Authorized Representative requirements.

July 9, 2026
Explained: How Vietnam Medical Device Registration Works (Timelines, Fees, & AR Strategy)
Malaysian dentist with a patient in a well lit dental clinic.
Breaking Into Southeast Asia’s Dental Market: 3 Things Manufacturers Need to Get Right

Enter Southeast Asia’s dental market with a clear strategy: navigate regulatory complexity, sequence market entry, and retain control of registrations to scale efficiently.

May 6, 2026
Breaking Into Southeast Asia’s Dental Market: 3 Things Manufacturers Need to Get Right
Cisema Logo: Navigating Regulation, Empowering Innovation
Cisema Launches a Redesigned Website

Learn about Cisema’s redesigned website with faster performance, clearer navigation and expanded Asia Pacific coverage.

May 6, 2026
Cisema Launches a Redesigned Website

Vietnam Temporarily Suspends New Food Registration Rules Under Resolution No. 15/2026/NQ-CP

Vietnam's temporary suspension of key food registration provisions creates a transitional regulatory environment, particularly affecting health supplement companies.

July 2, 2026
Vietnam Temporarily Suspends New Food Registration Rules Under Resolution No. 15/2026/NQ-CP
Vietnam Assigns MOH Oversight for Chemicals in Medical Products

Vietnam Assigns MOH Oversight for Chemicals in Medical Products

Vietnam's Decree No. 26/2026/ND-CP” confirms MoH oversight of chemicals in medical devices, IVDs, and medicines.

May 14, 2026
Vietnam Assigns MOH Oversight for Chemicals in Medical Products
Vietnam Strengthens Enforcement of Cosmetic Notification and PIF Compliance

Vietnam Strengthens Enforcement of Cosmetic Notification and PIF Compliance

Vietnam’s DAV intensifies inspections through March 2026, targeting cosmetic notification compliance and Product Information File readiness.

May 14, 2026
Vietnam Strengthens Enforcement of Cosmetic Notification and PIF Compliance
Vietnam Transfers High-Risk Medical Device Evaluation to Specialized Authorities

Vietnam Transfers High-Risk Medical Device Evaluation to Specialized Authorities

Vietnam’s Ministry of Health has delegated medical device oversight to specialized agencies, impacting registration and post-market surveillance.

May 14, 2026
Vietnam Transfers High-Risk Medical Device Evaluation to Specialized Authorities

Vietnam Cuts Advertising Red Tape for Healthcare Products

Vietnam’s MoH recently published Circular drops several healthcare advertising regulations and streamlines requirements for many categories.

April 23, 2026
Vietnam Cuts Advertising Red Tape for Healthcare Products
A top-down, flat-lay view of a white desk featuring a silver laptop with a blank screen. A person's hands are in the foreground holding two matte lipsticks in shades of red and dusty rose. The workspace is aesthetically arranged with various beauty items.

Vietnam Draft Cosmetic Decree Signals Tougher Compliance Environment

Vietnam’s draft cosmetic management decree would replace existing rules and strengthen post-market controls for cosmetic companies.

April 23, 2026
Vietnam Draft Cosmetic Decree Signals Tougher Compliance Environment
Two office professionals sit at a desk in an office reviewing cosmetic and skincare product packaging alongside printed documents and binders. One person examines a product bottle while the other works on a laptop, suggesting regulatory compliance review.

Vietnam Authorities Step Up Cosmetic Recalls as Enforcement Tightens

Vietnam’s Drug Administration (DAV) is stepping up cosmetic product recalls as post-market surveillance tightens.

April 23, 2026
Vietnam Authorities Step Up Cosmetic Recalls as Enforcement Tightens
Four professionals sit around a meeting table reviewing printed documents and binders related to product registration and regulatory compliance. A laptop screen displays “Product Registration Dossier,” while one person points to highlighted sections.

Vietnam Consolidates Medical Device Rules Under Decree 98 Framework

Vietnam’s Ministry of Health issued “Consolidated Document No. 08/VBHN-BYT (2026)”, unifying medical device regulations.

April 23, 2026
Vietnam Consolidates Medical Device Rules Under Decree 98 Framework

Vietnam Delays Implementation of New Health Supplement Regulations

Vietnam temporarily suspends implementation of stricter registration and import inspection rules for health supplement foods.

March 31, 2026
Vietnam Delays Implementation of New Health Supplement Regulations

Vietnam Formalizes Electronic Medical Device Procedures Under Decision 3830/QĐ-BYT

Vietnam’s Ministry of Health moves to standardize and digitize medical device administration, improving transparency and compliance.

March 31, 2026
Vietnam Formalizes Electronic Medical Device Procedures Under Decision 3830/QĐ-BYT

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