Local Authorised Representative in Vietnam

Entering Vietnam’s medical device market can be challenging, especially when navigating local regulations from overseas. That’s where Andaman Medical comes in.

As a trusted Local Authorised Representative (LAR) in Vietnam since 2017, we provide the local expertise and regulatory support you need to achieve smooth market access and ongoing compliance. We handle the complexities on your behalf, so you can focus on bringing your medical innovations to healthcare providers and patients across Vietnam.

Local Authorised Representative in Vietnam

In compliance with the Ministry of Health regulations, foreign manufacturers without a legal subsidiary in Vietnam must appoint a Local Authorised Representative (LAR), also known as an in-country representative or marketing authorisation holder.

Andaman Medical has served as a Local Authorised Representative in Vietnam since 2017.

Why Appoint a Local Authorised Representative (LAR) in Vietnam?

Appointing a Local Authorised Representative (LAR) in Vietnam isn’t just a regulatory formality—it’s a crucial step to ensure your medical device enters the market smoothly and achieves long-term success in this growing healthcare sector. Here’s why having a Local Authorised Representative (LAR) in Vietnam is essential:

At Andaman Medical, we specialise in providing trusted and professional LAR services tailored to Vietnam’s regulatory environment. With our in-depth knowledge of local requirements, we act as your dedicated in-country representative—ensuring full compliance, managing communication with the Vietnamese Ministry of Health (MoH), and overseeing all required post-market activities.

Here’s why having a Local Authorised Representative (LAR) in Vietnam is essential:

Why Appoint a Local Authorised Representative (LAR) in Vietnam?

As your marketing authorization holder or Authorised Representative Consultancy in the Philippines, Andaman Medical will:

Why Choose Andaman Medical for Your In-Country Representation in the Vietnam?

What You Need to Know About Having a Local Authorised Representative in Vietnam

To act as a Marketing Authorisation Holder (MAH) or Local Authorised Representative (LAR) in Vietnam, the following requirements must be met:

Licences

The in-country representative must obtain:

  • An Establishment License.
  • An Investment License.

Registration Accounts

The LAR must create accounts on the DMEC websites to register medical devices and in-vitro diagnostics with the Ministry of Health (MOH).

Eligibility and Certification

For handling medical devices of classes B, C, and D, the LAR must:

  • Apply for eligibility to trade these classes.
  • Obtain the Certificate of Medical Device Trading for classes B, C, and D.

 Appointment of Multiple In-Country Representatives

It is possible to appoint multiple in-country representatives in Vietnam. However, each LAR must individually register the device, and each registration is evaluated as a new application with corresponding registration fees.

Letter of Authorisation (LoA)

The foreign manufacturer must issue a Letter of Authorisation (LoA) according to the template in Circular 19/2021/TT/BYT, dated November 16, 2021. The LoA does not have a fixed duration.

Navigating the role of a Local Authorised Representative in Vietnam can be complex, but Andaman Medical is here to simplify the process and ensure you remain fully compliant. Connect with our experts today and take the first step toward seamless representation

Why Choose Andaman Medical for Your In-Country Representation in Vietnam?

As your Marketing Authorisation Holder or Authorised Representative Consultancy in Vietnam, Andaman Medical provides comprehensive services, including:

Regulatory Representation

Represent your company in all dealings with the Ministry of Health for medical devices and in-vitro diagnostics.

Product Registration and Importation

  • Register your medical devices with the Ministry of Health.
  • Facilitate product importation, including customs clearance, as Andaman Medical is also an Import License Holder.

Regulatory Submissions

  • Submit change notifications when required.
  • Ensure post-market surveillance, including Adverse Event Reporting.

Distributor Coordination

Maintain communication with your appointed distributors to ensure smooth operations and compliance.

Conformity Testing and Labelling

  • Ensure that required conformity testing is conducted.
  • Ensure medical devices or IVDs are labelled correctly, with information provided in Vietnamese.

Ministry of Health Liaison

  • Manage all communications with the Ministry of Health regarding your products.
  • Coordinate and assist with scheduling manufacturing facility inspections when necessary.

Local Presence

Operate a local office in Vietnam with telephone and email connectivity to ensure continuous support.

Regulatory Monitoring

Monitor regulatory developments and alert you to any changes or new regulations that may affect your products.

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