Backed by the expertise of Andaman Medical, our in-house team of regulatory affairs specialists provides unparalleled assistance to both Medical Devices and IVDs manufacturers and distributors. We boast a dedicated team of employees who offer steadfast support over the long-term.
As your in-country representative, we handle the entire spectrum of device registrations, from preparation to submission and ongoing management. This grants you independence and flexibility over market access and distribution strategy.
We offer more than just online registration; receive invaluable insight into navigating the complex regulatory landscape, especially amidst increased post-market surveillance and evolving compliance requirements. From customs clearance to end-customer distribution, we take care of the logistics, allowing you to focus on your business.
At Nord Pacific, we are committed to empowering you to thrive in the dynamic and ever-evolving Medical Devices and IVDs industry. Partner with us for comprehensive regulatory solutions and unlock your full potential in the market.
Our Mission
To enable Medical Devices and IVDs manufacturers and distributors to concentrate on their core business of developing and bringing medical devices & IVDs to market that improve the health and quality of life for millions. They can do this safe in the knowledge that they can rely on our dedicated Asia Regulatory Affairs Specialists team to register, represent and import their products.
Our Values
R for Responsibility
We have a legal, financial, environmental and social obligation to act correctly in respect of applicable local and international law. We are answerable not only to our clients, our colleagues but also to the legal frameworks in place, whilst respecting the environment and promoting social inclusion
I for Integrity
To enable medical device & IVD manufacturers and distributors to concentrate on their core business of developing and bringing medical devices & IVDs to market that improve the health and quality of life for millions. They can do this safe in the knowledge that they can rely on our dedicated Southeast Asia medical device consulting team to register, represent and import their products.
C for Collaboration
We pride ourselves on close collaboration with our local teams through open communication and developing personalized, long-term partnerships with our clients. What’s more we aim to reply to all client queries within 48 hours. So much so our client retention rate is a fantastic 94% as they choose to expand their reach in Southeast Asia by working with us in all of our country offices.
E for Energy
We are a rigorous team always looking to advance and improve what we do for our clients as well as colleagues, whilst maintaining the rigor and gravity required in the regulatory affairs industry.
Why Nord Pacific Medical?
Expert Guidance
In-house regulatory specialists ensure optimal market entry strategies for Medical Devices and IVDs without outsourcing.
End-to-End Support
Complete market access service, from registration to importation and delivery to your designated local distributor.
Responsive Partnership
Swift, personalized responses within 48 hours foster strong, enduring relationships.
Efficient Market Entry
Rapid, compliant market entry facilitated by our proactive regulatory monitoring and local expertise.
Localized Insight
Exclusive focus on the intricate local scene and a localized team provide unmatched regulatory support.
Empowered Control
Acting as in-country representatives, clients retain control over registrations and distribution strategies.
Accelerated Success
Speed up market entry by leveraging our regulatory expertise.
Innovation Enabled
Clients focus on innovation while relying on our team to manage their devices.
