Our Solutions

RegDesk Regulatory Intelligence

Every journey begins with a single step. The most important step to introducing your medical products to new markets is initial intelligence gathering. RegDesk saves time and reduces  risk by providing the most comprehensive, up-to-date regulatory intelligence on the web. Global medical device registration requirements are condensed into easy-to-follow steps and translated to English when necessary. 

Benefits of Using RegDesk Regulatory Intelligence

 

Problem: Regulatory requirements provided by national agencies are often filled with jargon, esoteric wording, and ambiguous classification descriptions. Translations to English are often poorly executed.

Solution:  Medical device registration guidelines provided by our platform are synthesized into easy-to -follow checklists and translated to English when necessary. We give you the information you need to move forward confidently with your application. 

Challenge: Sometimes even the most comprehensive regulatory intelligence still leaves questions.

Solution: RegDesk provides access to the largest network of regulatory consultants anywhere. Simply submit questions on your dashboard and receive insight from multiple industry experts within three weeks. Multiple opinions allow you to identify areas of consensus on difficult problems and move forward confidently with your submission.

 Problem: Regulatory requirements provided by national agencies are often filled with jargon, esoteric wording, and ambiguous classification descriptions. Translations to English are often poorly executed. 

Solution:  Medical device registration guidelines provided by our platform are synthesized into easy-to -follow checklists and translated to English when necessary. We give you the information you need to move forward confidently with your application. 

Challenge: Sometimes even the most comprehensive regulatory intelligence still leaves questions.

Solution: RegDesk provides access to the largest network of regulatory consultants anywhere. Simply submit questions on your dashboard and receive insight from multiple industry experts within three weeks. Multiple opinions allow you to identify areas of consensus on difficult problems and move forward confidently with your submission.

Why Choose US

The medical device industry is evolving quickly in response to recent innovations in communications and data processing technology. Relying on search engines or industry consultants to gather regulatory intelligence is as old-fashioned now as relying on print publications seemed ten years ago. Now is the time to adopt new solutions to age-old problems like expanding to foreign markets.