Top Post-Marketing Surveillance Companies in Vietnam

Top PMS Companies in Vietnam

Top Post-Marketing Surveillance Companies in Vietnam

Top Post-Marketing Surveillance Companies in Vietnam

After the approval and release of any medication and medical devices in the market, post-marketing surveillance plays a very significant role. It has been observed that the demand for post-market surveillance in Vietnam for medical products has increased significantly. Those pharmaceutical and healthcare companies that are looking to comply with local regulations and public safety have started to partner with top PMS companies in Vietnam.

If you are also looking for the best PMS Companies in Vietnam to associate with, you can go through this blog and find the company that suits your requirements best:

Best PMS Companies in Vietnam

1.IQVIA Vietnam:

Renowned globally, IQVIA doesn’t need an introduction for its services in healthcare data science and clinical research. In Vietnam, this company offers incredible post-market surveillance services. With the utilization of its comprehensive PMS solutions, you can receive high-quality data and insights to maintain regulatory compliance with the assurance of product safety. Its key services include product safety assessment, risk evaluation & mitigation strategies, and adverse event monitoring & reporting.

2.Spade Health:

Spade Health is another name for post-market surveillance in Vietnam. With the utilization of innovative research by Spade Health, you can get better insights to make the best-informed decisions. The PMS studies in Vietnam conducted by this company allow you to learn about the hazards you may be unaware of. Its main features are in-depth analysis and risk assessments. The in-depth analysis provided by experienced experts of Spade Health allows you to learn more about patterns, trends, and potential risks associated with medical products.

3.PharmaReg Solutions:

Another well-known consulting firm in Vietnam that offers PMS services in Vietnam and other parts of Southeast Asia. The main aim of this firm is to make sure that companies launching medical products meet the regulatory requirements of Vietnam. The major features of this company are post-market data collection & analysis, pharmacovigilance services, and real-time safety monitoring & reporting.

4.Pharmarack:

Based in Vietnam, Pharmarack understands the local needs, and hence, it offers post-market surveillance services tailored as per the requirements of the company. With the utilization of its proactive and reactive PMS services, clients can monitor the safety and efficiency of the product. The prime services offered by this company are risk management planning, PMS audits, quality control, regulatory consulting, and PMS documentation.

5. Asia Care Research:

Asia Care Research is a contract research Organization based in Vietnam. This company especially focuses on healthcare data collection including post-market surveillance. Well-known for its timely reporting, accurate data, and in-depth market analysis, this company offers tailored services as per the needs of the clients. Its main services are quality control, regulatory support, pharmacovigilance, and adverse event reporting.

Choosing the right partner for your post-market surveillance can be tough but essential, as you have to make sure your medical product complies with Vietnam’s regulatory requirements and maintains safety. The above list will help you to make the right decision, and you can monitor the efficacy and safety of your product.

FAQs: Post-Marketing Surveillance Companies in Vietnam

The best post-marketing surveillance companies in Vietnam provide pharmaceutical safety monitoring, adverse event reporting, pharmacovigilance support, medical device surveillance, and regulatory documentation. When selecting a provider, businesses should assess its local research capabilities, quality assurance procedures, healthcare professional network, reporting processes, and experience with Vietnam's regulatory requirements. Spade Health can also be considered for healthcare research support based on the scope of the project.
Post-marketing surveillance (PMS) involves monitoring the safety, performance, and effectiveness of medicines and medical devices after they enter the market. In Vietnam, PMS helps identify potential safety concerns, monitor adverse drug reactions, evaluate real-world product performance, and support appropriate regulatory action to protect patients.
Post-marketing surveillance companies may provide adverse event data collection, pharmacovigilance support, safety reporting, patient follow-up, healthcare professional interviews, real-world evidence research, medical device monitoring, and safety data analysis. The exact services depend on the provider's expertise and the product being monitored.
Pharmaceutical companies must follow applicable Vietnamese regulations concerning medicine safety monitoring, adverse drug reaction reporting, and the evaluation of safety and efficacy after marketing authorization. Requirements can vary by product category and regulatory instrument. Companies should confirm current obligations and reporting timelines with Vietnam's Ministry of Health and Drug Administration of Vietnam (DAV).
Post-marketing surveillance helps identify potential adverse drug reactions by collecting and analysing safety information from healthcare professionals, patients, medical literature, and other relevant sources. Researchers assess reported events for potential safety signals, enabling pharmaceutical companies to investigate risks and take appropriate follow-up action.
Post-marketing surveillance is the broader process of monitoring the safety and performance of products after they enter the market. Pharmacovigilance focuses specifically on detecting, assessing, understanding, and preventing adverse effects and other medicine-related problems. Pharmacovigilance is therefore an important component of post-marketing safety monitoring.
Post-market surveillance helps medical device manufacturers monitor device performance, identify malfunctions, collect user feedback, investigate complaints, and detect potential safety risks after commercial distribution. These insights can support corrective actions, risk management, product improvements, and compliance with applicable medical device regulations.
Real-world evidence provides insights into how medicines and medical devices perform in routine healthcare settings. By analysing relevant clinical records, observational studies, patient outcomes, and safety reports, organizations can identify emerging risks, assess treatment patterns, and better understand product performance beyond controlled clinical trials.
Companies should evaluate a potential partner's pharmacovigilance expertise, local regulatory knowledge, data security practices, quality management systems, reporting procedures, healthcare professional recruitment capabilities, and experience with similar products. It is also important to confirm whether the provider can support local-language data collection and the required reporting workflow.
Spade Health provides healthcare research and clinical research support across multiple regions, including Asia-Pacific. Depending on project requirements, its healthcare research capabilities may support data collection, healthcare professional research, patient insights, and evidence generation relevant to post-market research projects. Companies should confirm the availability of specific pharmacovigilance services, local fieldwork capabilities, and regulatory reporting support directly with the team.

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