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To leverage our team's expertise in regulatory, commercial and connection to assist our clients in global market strategy, resolving issue, complying with the regulatory requirement and obtaining approval to meet the quality, safety and effectiveness for medical devices, therapeutic and drugs usage. We aim to contribute our comprehensive services to Healthcare industry and MedTech community globally.​​
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Platform to connect Startups and companies to following stakeholders-

Investor

M&A Buyer

Clinician

Distributor

CDMO/OEM

Incubator/NGO

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Technical and Clinical compliance services, as well as Dashboard eQMS/eRMS for management of documents and registration status.

- Regulatory compliance

- Standard compliance

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Medtech Insight, Citeline Commercial

@Medtech_Insight

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EU Initiative Calls For Health App Assessments As Google And Apple ‘De Facto Regulators’...

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18 Jan 2023

What Clients Say

“ARQon has help AWAK achieve zero non-conformity during our ISO 13485: 2016 Quality Management Audit is not an easy feat to achieve. We like to thank them for their dedication and commitment in their work.”
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