“RegDesk Tracking has simplified the entire process. We no longer have to worry about missing deadlines on renewals. The best part is that we are able to generate reports with a click of a button.”

Regulatory Affairs Manager, Large Multinational
Corporation

Tracking and Monitoring Medical Device

RegDesk is the only lifecycle management platform for medical devices that includes AI-powered tracking software. Our platform eliminates the need to parse through endless spreadsheets for important information and eradicates the risk of human errors that can put products at risk.

 

Provides Guidance

Challenge:

The regulatory lifecycle for a single product can differ from market to market. Manually tracking numerous products marketed in multiple countries is a time consuming and tedious task that drains resources from other Regulatory Affairs projects. Failure to properly monitor submissions can lead to missed application renewal deadlines and products being pulled from market.

Solution:

RegDesk’s tracking software tracks all of your submissions simultaneously and delivers resubmission and change management alerts automatically, saving your regulatory intelligence team endless hours of parsing through spreadsheets.

Saves Time and Reduces Risk

Challenge:

Regulatory approval – as difficult as it is to achieve – is merely the first stage of a products lifecycle. What remains is the endless process of post-approval requirements, including postmarked surveillance and resubmissions. Because different nations have different post-approval requirements, the latter stage of your products lifecycle can be more challenging than the first.

Solution:

RegDesk’s AI-powered tracking software leverages the largest database of regulatory intelligence on the web to monitor the full lifecycle of your product in more than 115 markets around the world. Our data analysts continuously update our intel to reflect global regulatory changes so users always receive timely and accurate updates. RegDesk lifts the burden of regulatory research and oversight, so your team can focus on the product.

Saves Time and Reduces Risk

Challenge:

Regulatory approval – as difficult as it is to achieve – is merely the first stage of a products lifecycle. What remains is the endless process of post-approval requirements, including postmarked surveillance and resubmissions. Because different nations have different post-approval requirements, the latter stage of your products lifecycle can be more challenging than the first.

Solution:

: RegDesk’s AI-powered tracking software leverages the largest database of regulatory intelligence on the web to monitor the full lifecycle of your product in more than 115 markets around the world. Our data analysts continuously update our intel to reflect global regulatory changes so users always receive timely and accurate updates. RegDesk lifts the burden of regulatory research and oversight, so your team can focus on the product.

Why Choose US

There are many RIMS platforms on offer that allow you to store and manage your product and registration information, but RegDesk is much more than that. Our platform is the only regulatory management software solution that monitors the entire lifecycle of your products and alerts you when action is required. Staying updated is essential to successfully managing your products and RegDesk makes that easy.

 

Speak to a Regdesk Expert today!