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.
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.
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.