Clients

Where are we located?
ARQ-CLASS

Sales, Logistics & Others advisory and support

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Global Reach

ARQon has a GLOBAL team coming from various medical industries and regulatory authorities. Being receptive to local regulatory changes, we provide the best submission strategies for our clients.

Why 

CHOOSE 

ARQon?

Cost Effective

ARQon provides competitive costing as compared to other global consultants.

ARQon offers free and accurate resources. Please check out the links to our registration page by clicking on the respective countries below.

Fast Response

ARQon responds to any of your enquiries within short notice.  We do not like to keep a client waiting.

 
ARQon provides product registration on various countries based on each country's regulations. We can become your local license holder.
ARQon has a Medtech Business One-Stop Service (BOSS) team. We help manufacturers in sales and logistics.
ARQon provides extra QA/RA support, documentation & certification to help companies comply with internationally recognized standards.
ARQon provides technical documentation and compliance advisory to help manufacturers meet the design control requirements & build design history file.

ARQ®-10MDQ  "10 Questions for Medical Device Regulations and Answers"  for the countries is available.

Please contact us. 

The team was formed from individuals with vast experiences in medical device and drug manufacturing sites, trading industry and in regulatory authority.

"We like to thank them for their dedication and commitment in their work"

OUR TEAM

NEWS LIVE

 
 

It was confirmed by the European Commission on 30 October 2019 that the Medical Device Regulation (MDR) EUDAMED will be delayed for two years which will launch in May 2022.

The C...

Beginning of August, SFDA announced that the new system will replace the current MDMA system and more technical files will be required from the manufacturers to provide evidence...

As of 1 January 2018, non-corrective contact lens will be regulated as medical devices by the Medical Device Authority (MDA). According to the Medical Device (Declaration) Order...

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EVENTS & PROMOTIONS

PAsia and Indonesia Harapan Kita hospital
Medlab Asia
Hong Kong
Dusseldorf, Germany
Switzerland
SMF MTIG, APACMed, AdvaMed & US Trade
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NEWS BLOG

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Contact us by phone, email or fill up an enquiry form

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